Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: Regional experience and high incidence of carnitine deficiency

  1. Couce, M.L.
  2. Sánchez-Pintos, P.
  3. Diogo, L.
  4. Leão-Teles, E.
  5. Martins, E.
  6. Santos, H.
  7. Bueno, M.A.
  8. Delgado-Pecellín, C.
  9. Castiñeiras, D.E.
  10. Cocho, J.A.
  11. García-Villoria, J.
  12. Ribes, A.
  13. Fraga, J.M.
  14. Rocha, H.
Revista:
Orphanet Journal of Rare Diseases

ISSN: 1750-1172

Ano de publicación: 2013

Volume: 8

Número: 1

Tipo: Artigo

DOI: 10.1186/1750-1172-8-102 GOOGLE SCHOLAR lock_openAcceso aberto editor