Genotype-phenotype correlation in vanishing white matter disease-Reference-Cited by-同舟云学术

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Genotype-phenotype correlation in vanishing white matter disease

Published:2010-10-25 Issue:17 Volume:75 Page:1555-1559
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

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

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 57 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Adult-onset leukoencephalopathy with vanishing white matter with compound heterozygous EIF2B3 gene variants;BMC Neurology;2024-06-13

2. In vivo base editing of a pathogenic Eif2b5 variant improves vanishing white matter phenotypes in mice;Molecular Therapy;2024-05

3. Core protocol development for phase 2/3 clinical trials in the leukodystrophy vanishing white matter: a consensus statement by the VWM consortium and patient advocates;BMC Neurology;2023-08-17

4. A novel missense variant in EIF2B5 identified in a consanguineous Iranian family with vanishing white matter disease and a brief review of the literature;Journal of Genetics;2023-08-07

5. Clinical, genetic, and molecular characteristics in a central‐southern Chinese cohort of genetic leukodystrophies;Annals of Clinical and Translational Neurology;2023-07-11

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