Erratum: LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance (Brain (2016) 139 (782-794) DOI: 10.1093/brain/awv392)

Cristina Dallabona, Truus E. M. Abbink, Rosalba Carrozzo, Alessandra Torraco, Andrea Legati, Carola G. M. van Berkel, Marcello Niceta, Tiziana Langella, Daniela Verrigni, Teresa Rizza, Daria Diodato, Fiorella Piemonte, Eleonora Lamantea, Mingyan Fang, Jianguo Zhang, Diego Martinelli, Elsa Bevivino, Carlo Dionisi-Vici, Adeline Vanderver, Sunny G. Philip & 14 others Manju A. Kurian, Ishwar C. Verma, Sunita Bijarnia-Mahay, Sandra Jacinto, Fatima Furtado, Patrizia Accorsi, Anna Ardissone, Isabella Moroni, Ileana Ferrero, Marco Tartaglia, Paola Goffrini, Daniele Ghezzi, Marjo S. van der Knaap, Enrico Bertini

Research output: Contribution to journalErratumAcademicpeer-review

Abstract

Cristina Dallabona, Truus E. M. Abbink, Rosalba Carrozzo, Alessandra Torraco, Andrea Legati, Carola G. M. van Berkel, Marcello Niceta, Tiziana Langella, Daniela Verrigni, Teresa Rizza, Daria Diodato, Fiorella Piemonte, Eleonora Lamantea, Mingyan Fang, Jianguo Zhang, Diego Martinelli, Elsa Bevivino, Carlo Dionisi-Vici, Adeline Vanderver, Sunny G. Philip, Manju A. Kurian, Ishwar C. Verma, Sunita Bijarnia-Mahay, Sandra Jacinto, Fatima Furtado, Patrizia Accorsi, Anna Ardissone, Isabella Moroni, Ileana Ferrero, Marco Tartaglia, Paola Goffrini, Daniele Ghezzi, Marjo S. van der Knaap and Enrico Bertini. LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance. Brain 2016; 139: 782-794. doi:10.1093/brain/awv392. The authors apologize for mixing the mutations of Patients 5 and 7 on pages 788 and 789 in Figure 2 and its legend, in the main text and the online Supplementary Tables. This has now been corrected online. On page 788, the text should read: Sanger sequencing of the entire coding sequence of LYRM7 and intron-exon boundaries was performed in three additional patients. Patient 5 was found homozygous for the c.37delA (p.Thr13Hisfs∗17) mutation, which is predicted to dramatically affect recognition of the splice donor motif of exon 4 and likely impair proper RNA splicing (Fig. 2M and N), while Patients 6 and 7 were found to be homozygous for the c.214C4T (p.Q72∗) (Fig. 2L), and c.243-244 + 2delGAGT (p.?) (Fig. 2H) mutations, respectively. The Supplementary Tables have been corrected online. On page 789, Figure 2 and legend should be as follows.
Original languageEnglish
Pages (from-to)e82
JournalBrain
Volume141
Issue number11
DOIs
Publication statusPublished - 2018

Cite this

Dallabona, Cristina ; Abbink, Truus E. M. ; Carrozzo, Rosalba ; Torraco, Alessandra ; Legati, Andrea ; van Berkel, Carola G. M. ; Niceta, Marcello ; Langella, Tiziana ; Verrigni, Daniela ; Rizza, Teresa ; Diodato, Daria ; Piemonte, Fiorella ; Lamantea, Eleonora ; Fang, Mingyan ; Zhang, Jianguo ; Martinelli, Diego ; Bevivino, Elsa ; Dionisi-Vici, Carlo ; Vanderver, Adeline ; Philip, Sunny G. ; Kurian, Manju A. ; Verma, Ishwar C. ; Bijarnia-Mahay, Sunita ; Jacinto, Sandra ; Furtado, Fatima ; Accorsi, Patrizia ; Ardissone, Anna ; Moroni, Isabella ; Ferrero, Ileana ; Tartaglia, Marco ; Goffrini, Paola ; Ghezzi, Daniele ; van der Knaap, Marjo S. ; Bertini, Enrico. / Erratum: LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance (Brain (2016) 139 (782-794) DOI: 10.1093/brain/awv392). In: Brain. 2018 ; Vol. 141, No. 11. pp. e82.
@article{558bcade4f1140368ce3d27de4a51be7,
title = "Erratum: LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance (Brain (2016) 139 (782-794) DOI: 10.1093/brain/awv392)",
abstract = "Cristina Dallabona, Truus E. M. Abbink, Rosalba Carrozzo, Alessandra Torraco, Andrea Legati, Carola G. M. van Berkel, Marcello Niceta, Tiziana Langella, Daniela Verrigni, Teresa Rizza, Daria Diodato, Fiorella Piemonte, Eleonora Lamantea, Mingyan Fang, Jianguo Zhang, Diego Martinelli, Elsa Bevivino, Carlo Dionisi-Vici, Adeline Vanderver, Sunny G. Philip, Manju A. Kurian, Ishwar C. Verma, Sunita Bijarnia-Mahay, Sandra Jacinto, Fatima Furtado, Patrizia Accorsi, Anna Ardissone, Isabella Moroni, Ileana Ferrero, Marco Tartaglia, Paola Goffrini, Daniele Ghezzi, Marjo S. van der Knaap and Enrico Bertini. LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance. Brain 2016; 139: 782-794. doi:10.1093/brain/awv392. The authors apologize for mixing the mutations of Patients 5 and 7 on pages 788 and 789 in Figure 2 and its legend, in the main text and the online Supplementary Tables. This has now been corrected online. On page 788, the text should read: Sanger sequencing of the entire coding sequence of LYRM7 and intron-exon boundaries was performed in three additional patients. Patient 5 was found homozygous for the c.37delA (p.Thr13Hisfs∗17) mutation, which is predicted to dramatically affect recognition of the splice donor motif of exon 4 and likely impair proper RNA splicing (Fig. 2M and N), while Patients 6 and 7 were found to be homozygous for the c.214C4T (p.Q72∗) (Fig. 2L), and c.243-244 + 2delGAGT (p.?) (Fig. 2H) mutations, respectively. The Supplementary Tables have been corrected online. On page 789, Figure 2 and legend should be as follows.",
author = "Cristina Dallabona and Abbink, {Truus E. M.} and Rosalba Carrozzo and Alessandra Torraco and Andrea Legati and {van Berkel}, {Carola G. M.} and Marcello Niceta and Tiziana Langella and Daniela Verrigni and Teresa Rizza and Daria Diodato and Fiorella Piemonte and Eleonora Lamantea and Mingyan Fang and Jianguo Zhang and Diego Martinelli and Elsa Bevivino and Carlo Dionisi-Vici and Adeline Vanderver and Philip, {Sunny G.} and Kurian, {Manju A.} and Verma, {Ishwar C.} and Sunita Bijarnia-Mahay and Sandra Jacinto and Fatima Furtado and Patrizia Accorsi and Anna Ardissone and Isabella Moroni and Ileana Ferrero and Marco Tartaglia and Paola Goffrini and Daniele Ghezzi and {van der Knaap}, {Marjo S.} and Enrico Bertini",
year = "2018",
doi = "10.1093/brain/awy194",
language = "English",
volume = "141",
pages = "e82",
journal = "Brain",
issn = "0006-8950",
publisher = "Oxford University Press",
number = "11",

}

Dallabona, C, Abbink, TEM, Carrozzo, R, Torraco, A, Legati, A, van Berkel, CGM, Niceta, M, Langella, T, Verrigni, D, Rizza, T, Diodato, D, Piemonte, F, Lamantea, E, Fang, M, Zhang, J, Martinelli, D, Bevivino, E, Dionisi-Vici, C, Vanderver, A, Philip, SG, Kurian, MA, Verma, IC, Bijarnia-Mahay, S, Jacinto, S, Furtado, F, Accorsi, P, Ardissone, A, Moroni, I, Ferrero, I, Tartaglia, M, Goffrini, P, Ghezzi, D, van der Knaap, MS & Bertini, E 2018, 'Erratum: LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance (Brain (2016) 139 (782-794) DOI: 10.1093/brain/awv392)' Brain, vol. 141, no. 11, pp. e82. https://doi.org/10.1093/brain/awy194

Erratum: LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance (Brain (2016) 139 (782-794) DOI: 10.1093/brain/awv392). / Dallabona, Cristina; Abbink, Truus E. M.; Carrozzo, Rosalba; Torraco, Alessandra; Legati, Andrea; van Berkel, Carola G. M.; Niceta, Marcello; Langella, Tiziana; Verrigni, Daniela; Rizza, Teresa; Diodato, Daria; Piemonte, Fiorella; Lamantea, Eleonora; Fang, Mingyan; Zhang, Jianguo; Martinelli, Diego; Bevivino, Elsa; Dionisi-Vici, Carlo; Vanderver, Adeline; Philip, Sunny G.; Kurian, Manju A.; Verma, Ishwar C.; Bijarnia-Mahay, Sunita; Jacinto, Sandra; Furtado, Fatima; Accorsi, Patrizia; Ardissone, Anna; Moroni, Isabella; Ferrero, Ileana; Tartaglia, Marco; Goffrini, Paola; Ghezzi, Daniele; van der Knaap, Marjo S.; Bertini, Enrico.

In: Brain, Vol. 141, No. 11, 2018, p. e82.

Research output: Contribution to journalErratumAcademicpeer-review

TY - JOUR

T1 - Erratum: LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance (Brain (2016) 139 (782-794) DOI: 10.1093/brain/awv392)

AU - Dallabona, Cristina

AU - Abbink, Truus E. M.

AU - Carrozzo, Rosalba

AU - Torraco, Alessandra

AU - Legati, Andrea

AU - van Berkel, Carola G. M.

AU - Niceta, Marcello

AU - Langella, Tiziana

AU - Verrigni, Daniela

AU - Rizza, Teresa

AU - Diodato, Daria

AU - Piemonte, Fiorella

AU - Lamantea, Eleonora

AU - Fang, Mingyan

AU - Zhang, Jianguo

AU - Martinelli, Diego

AU - Bevivino, Elsa

AU - Dionisi-Vici, Carlo

AU - Vanderver, Adeline

AU - Philip, Sunny G.

AU - Kurian, Manju A.

AU - Verma, Ishwar C.

AU - Bijarnia-Mahay, Sunita

AU - Jacinto, Sandra

AU - Furtado, Fatima

AU - Accorsi, Patrizia

AU - Ardissone, Anna

AU - Moroni, Isabella

AU - Ferrero, Ileana

AU - Tartaglia, Marco

AU - Goffrini, Paola

AU - Ghezzi, Daniele

AU - van der Knaap, Marjo S.

AU - Bertini, Enrico

PY - 2018

Y1 - 2018

N2 - Cristina Dallabona, Truus E. M. Abbink, Rosalba Carrozzo, Alessandra Torraco, Andrea Legati, Carola G. M. van Berkel, Marcello Niceta, Tiziana Langella, Daniela Verrigni, Teresa Rizza, Daria Diodato, Fiorella Piemonte, Eleonora Lamantea, Mingyan Fang, Jianguo Zhang, Diego Martinelli, Elsa Bevivino, Carlo Dionisi-Vici, Adeline Vanderver, Sunny G. Philip, Manju A. Kurian, Ishwar C. Verma, Sunita Bijarnia-Mahay, Sandra Jacinto, Fatima Furtado, Patrizia Accorsi, Anna Ardissone, Isabella Moroni, Ileana Ferrero, Marco Tartaglia, Paola Goffrini, Daniele Ghezzi, Marjo S. van der Knaap and Enrico Bertini. LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance. Brain 2016; 139: 782-794. doi:10.1093/brain/awv392. The authors apologize for mixing the mutations of Patients 5 and 7 on pages 788 and 789 in Figure 2 and its legend, in the main text and the online Supplementary Tables. This has now been corrected online. On page 788, the text should read: Sanger sequencing of the entire coding sequence of LYRM7 and intron-exon boundaries was performed in three additional patients. Patient 5 was found homozygous for the c.37delA (p.Thr13Hisfs∗17) mutation, which is predicted to dramatically affect recognition of the splice donor motif of exon 4 and likely impair proper RNA splicing (Fig. 2M and N), while Patients 6 and 7 were found to be homozygous for the c.214C4T (p.Q72∗) (Fig. 2L), and c.243-244 + 2delGAGT (p.?) (Fig. 2H) mutations, respectively. The Supplementary Tables have been corrected online. On page 789, Figure 2 and legend should be as follows.

AB - Cristina Dallabona, Truus E. M. Abbink, Rosalba Carrozzo, Alessandra Torraco, Andrea Legati, Carola G. M. van Berkel, Marcello Niceta, Tiziana Langella, Daniela Verrigni, Teresa Rizza, Daria Diodato, Fiorella Piemonte, Eleonora Lamantea, Mingyan Fang, Jianguo Zhang, Diego Martinelli, Elsa Bevivino, Carlo Dionisi-Vici, Adeline Vanderver, Sunny G. Philip, Manju A. Kurian, Ishwar C. Verma, Sunita Bijarnia-Mahay, Sandra Jacinto, Fatima Furtado, Patrizia Accorsi, Anna Ardissone, Isabella Moroni, Ileana Ferrero, Marco Tartaglia, Paola Goffrini, Daniele Ghezzi, Marjo S. van der Knaap and Enrico Bertini. LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance. Brain 2016; 139: 782-794. doi:10.1093/brain/awv392. The authors apologize for mixing the mutations of Patients 5 and 7 on pages 788 and 789 in Figure 2 and its legend, in the main text and the online Supplementary Tables. This has now been corrected online. On page 788, the text should read: Sanger sequencing of the entire coding sequence of LYRM7 and intron-exon boundaries was performed in three additional patients. Patient 5 was found homozygous for the c.37delA (p.Thr13Hisfs∗17) mutation, which is predicted to dramatically affect recognition of the splice donor motif of exon 4 and likely impair proper RNA splicing (Fig. 2M and N), while Patients 6 and 7 were found to be homozygous for the c.214C4T (p.Q72∗) (Fig. 2L), and c.243-244 + 2delGAGT (p.?) (Fig. 2H) mutations, respectively. The Supplementary Tables have been corrected online. On page 789, Figure 2 and legend should be as follows.

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UR - https://www.ncbi.nlm.nih.gov/pubmed/30137257

U2 - 10.1093/brain/awy194

DO - 10.1093/brain/awy194

M3 - Erratum

VL - 141

SP - e82

JO - Brain

JF - Brain

SN - 0006-8950

IS - 11

ER -