Caso clínico
Asociación entre la mutación homocigota c.318A>T en el exón 2 del gen EIF2B5 y la forma infantil de la leucoencefalopatía con sustancia blanca evanescente
Association between homozygous c.318A>GT mutation in exon 2 of the EIF2B5 gene and the infantile form of vanishing white matter leukoencephalopathy
Carmen Esmera, Gabriela Blanco Hernándezb, Víctor Saavedra Alanísc, Jorge Guillermo Reyes Vacad, Antonio Bravo Orob,
Autor para correspondencia
a Departamento de Genética, Hospital Central Dr. Ignacio Morones Prieto, San Luis Potosí, San Luis Potosí, México
b Departamento de Neuropediatría, Hospital Central Dr. Ignacio Morones Prieto, San Luis Potosí, San Luis Potosí, México
c Departamento de Biología Molecular, Facultad de Medicina de la Universidad Autónoma de San Luis Potosí, San Luis Potosí, San Luis Potosí, México
d Departamento de Radiología e Imagen, Hospital Central Dr. Ignacio Morones Prieto, San Luis Potosí, San Luis Potosí, México
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