Cargando…
A Novel Mutation in the EIF2B4 Gene Associated with Leukoencephalopathy with Vanishing White Matter
Autores principales: | Hettiaracchchi, D., Neththikumara, N., Pathirana, B. A. P. S., Padeniya, A., Dissanayake, V. H. W. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057309/ https://www.ncbi.nlm.nih.gov/pubmed/30073106 http://dx.doi.org/10.1155/2018/2731039 |
Ejemplares similares
-
Vanishing white matter leukodystrophy due to novel EIF2B4 mutation in an adult female
por: Goyal, Sheetal, et al.
Publicado: (2023) -
Fifteen Novel EIF2B1-5 Mutations Identified in Chinese Children with Leukoencephalopathy with Vanishing White Matter and a Long Term Follow-Up
por: Zhang, Haihua, et al.
Publicado: (2015) -
Identification of a Novel Heterozygous Mutation in the EIF2B4 Gene Associated With Vanishing White Matter Disease
por: Tian, Yun, et al.
Publicado: (2022) -
Leukoencephalopathy with vanishing white matter disease: a case report study
por: Kami, Atefe, et al.
Publicado: (2023) -
Association Between Late-Onset Leukoencephalopathy With Vanishing White Matter and Compound Heterozygous EIF2B5 Gene Mutations: A Case Report and Review of the Literature
por: Kong, Fanxin, et al.
Publicado: (2022)