Hypermethioninaemia due to methionine adenosyltransferase I/III (MAT I/III) deficiency: Diagnosis in an expanded neonatal screening programme

  1. Couce, M.L.
  2. Bóveda, M.D.
  3. Castiñeiras, D.E.
  4. Corrales, F.J.
  5. Mora, M.I.
  6. Fraga, J.M.
  7. Mudd, S.H.
Revista:
Journal of Inherited Metabolic Disease

ISSN: 1573-2665 0141-8955

Ano de publicación: 2008

Volume: 31

Número: SUPPL. 2

Tipo: Artigo

DOI: 10.1007/S10545-008-0811-3 GOOGLE SCHOLAR