Rare FOXC1 variants in congenital glaucoma: Identification of translation regulatory sequences

  1. Medina-Trillo, C.
  2. Aroca-Aguilar, J.-D.
  3. Méndez-Hernández, C.-D.
  4. Morales, L.
  5. García-Antón, M.
  6. García-Feijoo, J.
  7. Escribano, J.
Aldizkaria:
European Journal of Human Genetics

ISSN: 1476-5438,  1018-4813

Argitalpen urtea: 2016

Alea: 24

Zenbakia: 5

Orrialdeak: 672-680

Mota: Artikulua

DOI: 10.1038/EJHG.2015.169 GOOGLE SCHOLAR lock_openSarbide irekia editor
Datuen iturria: Scopus