[Association between homozygous c.318A>GT mutation in exon 2 of the EIF2B5 gene and the infantile form of vanishing white matter leukoencephalopathy]. [electronic resource]

By: Contributor(s): Producer: 20190501Description: 364-369 p. digitalISSN:
  • 1665-1146
Subject(s): Online resources: In: Boletin medico del Hospital Infantil de Mexico vol. 74
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Publication Type: Case Reports; Journal Article

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