UFM1 founder mutation in the Roma population causes severe variant of Hypomyelination with Atrophy of the Basal ganglia and Cerebellum (H-ABC)

E. M. Hamilton, E. Bertini, L. Kalaydjieva, B. Morar, D. Dojcakova, D. Diodato, N. Wolf, Q. Waisfisz, E. Abbink, M. S. van der Knaap

Research output: Contribution to journalMeeting AbstractAcademic

Original languageEnglish
Pages (from-to)31-32
JournalEuropean Journal of Neurology
Volume25
Publication statusPublished - Jun 2018

Cite this

@article{287eb9c523d24f4484efd0cc93c09501,
title = "UFM1 founder mutation in the Roma population causes severe variant of Hypomyelination with Atrophy of the Basal ganglia and Cerebellum (H-ABC)",
author = "Hamilton, {E. M.} and E. Bertini and L. Kalaydjieva and B. Morar and D. Dojcakova and D. Diodato and N. Wolf and Q. Waisfisz and E. Abbink and {van der Knaap}, {M. S.}",
year = "2018",
month = "6",
language = "English",
volume = "25",
pages = "31--32",
journal = "European Journal of Neurology",
issn = "1351-5101",
publisher = "Wiley-Blackwell",

}

UFM1 founder mutation in the Roma population causes severe variant of Hypomyelination with Atrophy of the Basal ganglia and Cerebellum (H-ABC). / Hamilton, E. M.; Bertini, E.; Kalaydjieva, L.; Morar, B.; Dojcakova, D.; Diodato, D.; Wolf, N.; Waisfisz, Q.; Abbink, E.; van der Knaap, M. S.

In: European Journal of Neurology, Vol. 25, 06.2018, p. 31-32.

Research output: Contribution to journalMeeting AbstractAcademic

TY - JOUR

T1 - UFM1 founder mutation in the Roma population causes severe variant of Hypomyelination with Atrophy of the Basal ganglia and Cerebellum (H-ABC)

AU - Hamilton, E. M.

AU - Bertini, E.

AU - Kalaydjieva, L.

AU - Morar, B.

AU - Dojcakova, D.

AU - Diodato, D.

AU - Wolf, N.

AU - Waisfisz, Q.

AU - Abbink, E.

AU - van der Knaap, M. S.

PY - 2018/6

Y1 - 2018/6

M3 - Meeting Abstract

VL - 25

SP - 31

EP - 32

JO - European Journal of Neurology

JF - European Journal of Neurology

SN - 1351-5101

ER -