2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: An X-linked inborn error of isoleucine metabolism that may mimic a mitochondrial disease
- García-Villoria, J.
- Ofman, R.
- Sala, P.R.
- Merinero, B.
- Ramos, J.
- García-Silva, M.T.
- Beseler, B.
- Dalmau, J.
- Wanders, R.J.A.
- Ugarte, M.
- Ribes, A.
ISSN: 0031-3998
Argitalpen urtea: 2005
Alea: 58
Zenbakia: 3
Orrialdeak: 488-491
Mota: Artikulua