Genotype-phenotype correlation in vanishing white matter disease

H.D.W. van der Lei; C.G.M. van Berkel; W.N. van Wieringen; C. Brenner; A. Feigenbaum; S. Mercimek-Mahmutoglu; M. Philippart; B. Tatli; E. Wassmer; G.C. Scheper; M.S. van der Knaap

doi:10.1212/WNL.0b013e3181f962ae

Genotype-phenotype correlation in vanishing white matter disease

H.D.W. van der Lei, C.G.M. van Berkel, W.N. van Wieringen, C. Brenner, A. Feigenbaum, S. Mercimek-Mahmutoglu, M. Philippart, B. Tatli, E. Wassmer, G.C. Scheper, M.S. van der Knaap

Research output: Contribution to journal › Article › Academic › peer-review

Original language	Undefined/Unknown
Pages (from-to)	1555-1559
Journal	Neurology
Volume	75
Issue number	17
DOIs	https://doi.org/10.1212/WNL.0b013e3181f962ae
Publication status	Published - 2010

Access to Document

10.1212/WNL.0b013e3181f962ae

Cite this

@article{9dee627e87a3498fb79c62b373ee601e,

title = "Genotype-phenotype correlation in vanishing white matter disease",

author = "{van der Lei}, H.D.W. and {van Berkel}, C.G.M. and {van Wieringen}, W.N. and C. Brenner and A. Feigenbaum and S. Mercimek-Mahmutoglu and M. Philippart and B. Tatli and E. Wassmer and G.C. Scheper and {van der Knaap}, M.S.",

year = "2010",

doi = "10.1212/WNL.0b013e3181f962ae",

language = "Undefined/Unknown",

volume = "75",

pages = "1555--1559",

journal = "Neurology",

issn = "0028-3878",

publisher = "Lippincott Williams and Wilkins",

number = "17",

}

TY - JOUR

T1 - Genotype-phenotype correlation in vanishing white matter disease

AU - van der Lei, H.D.W.

AU - van Berkel, C.G.M.

AU - van Wieringen, W.N.

AU - Brenner, C.

AU - Feigenbaum, A.

AU - Mercimek-Mahmutoglu, S.

AU - Philippart, M.

AU - Tatli, B.

AU - Wassmer, E.

AU - Scheper, G.C.

AU - van der Knaap, M.S.

PY - 2010

Y1 - 2010

U2 - 10.1212/WNL.0b013e3181f962ae

DO - 10.1212/WNL.0b013e3181f962ae

M3 - Article

C2 - 20975056

VL - 75

SP - 1555

EP - 1559

JO - Neurology

JF - Neurology

SN - 0028-3878

IS - 17

ER -