A rare mutation in EIF2B4 gene in an epileptic child with vanishing white matter disease: a case report.

Gungor, O

A rare mutation in EIF2B4 gene in an epileptic child with vanishing white matter disease: a case report. [electronic resource] - Genetic counseling (Geneva, Switzerland) 2015 - 41-6 p. digital

Publication Type: Case Reports; Journal Article

1015-8146


Epilepsy--genetics
Eukaryotic Initiation Factor-2B--genetics
Humans
Infant
Leukoencephalopathies--genetics
Male
Mutation