2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: An X-linked inborn error of isoleucine metabolism that may mimic a mitochondrial disease

  1. García-Villoria, J.
  2. Ofman, R.
  3. Sala, P.R.
  4. Merinero, B.
  5. Ramos, J.
  6. García-Silva, M.T.
  7. Beseler, B.
  8. Dalmau, J.
  9. Wanders, R.J.A.
  10. Ugarte, M.
  11. Ribes, A.
Aldizkaria:
Pediatric Research

ISSN: 0031-3998

Argitalpen urtea: 2005

Alea: 58

Zenbakia: 3

Orrialdeak: 488-491

Mota: Artikulua

DOI: 10.1203/01.PDR.0000176916.94328.CD GOOGLE SCHOLAR lock_openSarbide irekia editor
Datuen iturria: Scopus