[Ketoacidotic coma in an infant as the form of onset of a mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency].

Autor: Yeste Fernández D; Laboratorio de Metabolopatías, Hospital Universitari Materno Infantil Vall d'Hebron, Barcelona., Castelló Girona F, Mora Graupera J, Riudor Taravila E, Arranz Amo J, Ribes Rubió A, Pérez Cerdá C

Publikováno v: Anales espanoles de pediatria [An Esp Pediatr] 1996 Jun; Vol. 44 (6), pp. 620-2.