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Déficit del cofactor molibdeno como causa de encefalopatía epiléptica precoz
A. Palacios Cuestaa,†, M.T. García Silvaa, J. Sánchez del Pozob, A. Nogales Espertc, A. Puche Mirad, M. Ugarte Péreze
a Unidad de Enfermedades Metabólicas y Mitocondriales. Departamento de Pediatría
b Unidad de Sindromología. Departamento de Pediatría. Hospital Universitario 12 de Octubre. Madrid
c Departamento de Pediatría. Hospital Universitario 12 de Octubre. Madrid
d Servicio de Neuropediatría. Hospital Virgen de la Arrixaca. Murcia
e Centro de Diagnóstico de Enfermedades Moleculares. Facultad de Ciencias. Universidad Autónoma. Madrid. España
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Información del artículo
ISSN: 16954033Idioma original: Español
DOI:10.1157/13124906
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