Biochemical effects of mutations in the gene encoding the alpha subunit of eukaryotic initiation factor (eIF) 2B associated with Vanishing White Matter disease

BACKGROUND: Leukoencephalopathy with Vanishing White Matter (VWM) is an autosomal recessive disorder caused by germline mutations in the genes EIF2B1-5, which encode the 5 subunits of the eukaryotic translation initiation factor eIF2B. To date, analysis of the biochemical effects of mutations in the...

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Detalles Bibliográficos
Autores principales: Wortham, Noel C., Proud, Christopher G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593227/
https://www.ncbi.nlm.nih.gov/pubmed/26285592
http://dx.doi.org/10.1186/s12881-015-0204-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593227/
https://www.ncbi.nlm.nih.gov/pubmed/26285592
http://dx.doi.org/10.1186/s12881-015-0204-z

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