PRPH2-related retinal diseases: Broadening the clinical spectrum and describing a new mutation

  1. Coco-Martin, R.M.
  2. Sanchez-Tocino, H.T.
  3. Desco, C.
  4. Usategui-Martín, R.
  5. Tellería, J.J.
Aldizkaria:
Genes

ISSN: 2073-4425

Argitalpen urtea: 2020

Alea: 11

Zenbakia: 7

Orrialdeak: 1-24

Mota: Artikulua

DOI: 10.3390/GENES11070773 GOOGLE SCHOLAR lock_openSarbide irekia editor
Datuen iturria: Scopus