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2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase (MHBD) Deficiency: An X-linked Inborn Error of Isoleucine Metabolism that May Mimic a Mitochondrial Disease
Perez-Cerda, Celia, García-Villoria, Judit, Ofman, Rob, Sala, Pedro Ruiz, Merinero, Begoña, Ramos, Julio, García-Silva, Maria Teresa, Beseler, Beatriz, Dalmau, Jaime, Wanders, Ronald J A, Ugarte, MagdVolume:
58
Language:
english
Journal:
Pediatric Research
DOI:
10.1203/01.pdr.0000176916.94328.cd
Date:
September, 2005
File:
PDF, 165 KB
english, 2005