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

C. Esmer, Gabriela Blanco-Hernández, V. Saavedra-Alanis, J. Reyes-Vaca, A. Bravo-Oro
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EIF2B5基因外显子2纯合c.318A>GT突变与婴儿型消失性白质脑白质病的关系
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