A novel congenital disorder of glycosylation type without central nervous system involvement caused by mutations in the phosphoglucomutase 1 gene

  1. Pérez, B.
  2. Medrano, C.
  3. Ecay, M.J.
  4. Ruiz-Sala, P.
  5. Martínez-Pardo, M.
  6. Ugarte, M.
  7. Pérez-Cerdá, C.
Aldizkaria:
Journal of Inherited Metabolic Disease

ISSN: 0141-8955,  1573-2665

Argitalpen urtea: 2013

Alea: 36

Zenbakia: 3

Orrialdeak: 535-542

Mota: Artikulua

DOI: 10.1007/S10545-012-9525-7 GOOGLE SCHOLAR

Garapen Iraunkorreko Helburuak