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.
Journal:
American Journal of Medical Genetics, Part A

ISSN: 1552-4825,  1552-4833

Year of publication: 2007

Volume: 143

Issue: 9

Pages: 916-920

Type: Article

DOI: 10.1002/AJMG.A.31521 GOOGLE SCHOLAR
Data source: Scopus