Genetic analysis of 2299delG and C759F mutations (USH2A) in patients with visual and/or auditory impairments

  1. Aller, E.
  2. Nájera, C.
  3. Millán, J.M.
  4. Oltra, J.S.
  5. Pérez-Garrigues, H.
  6. Vilela, C.
  7. Navea, A.
  8. Beneyto, M.
Aldizkaria:
European Journal of Human Genetics

ISSN: 1018-4813

Argitalpen urtea: 2004

Alea: 12

Zenbakia: 5

Orrialdeak: 407-410

Mota: Artikulua

DOI: 10.1038/SJ.EJHG.5201138 GOOGLE SCHOLAR lock_openSarbide irekia editor
Datuen iturria: Scopus