Contiguous deletion of the NDP, MAOA, MAOB and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy

  1. Rodriguez-Revenga, L.
  2. Madrigal, I.
  3. Alkhalidi, L.S.
  4. Armengol, L.
  5. González, E.
  6. Badenas, C.
  7. Estivill, X.
  8. Milà, M.
Aldizkaria:
American Journal of Medical Genetics, Part A

ISSN: 1552-4825,  1552-4833

Argitalpen urtea: 2007

Alea: 143

Zenbakia: 9

Orrialdeak: 916-920

Mota: Artikulua

DOI: 10.1002/AJMG.A.31521 GOOGLE SCHOLAR
Datuen iturria: Scopus