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PRPH2 mutation c.582-1G>A causing adult-onset macular dystrophy with a benign concentric annular macular dystrophy phenotype in a family.
Fernández-Berdasco, Karina; Galvez-Olortegui, José; Guillén-Lozada, Sussan's Pamela; González, Noelia García; Castro-Navarro, Joaquín.
Afiliação
  • Fernández-Berdasco K; Ophthalmology Department, Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Galvez-Olortegui J; Ophthalmology Department, Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Guillén-Lozada SP; Evidence Based Ophthalmology Unit (Oftalmoevidencia), Scientia Clinical and Epidemiological Research Institute, Trujillo, Peru.
  • González NG; Ophthalmology Department, Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Castro-Navarro J; Genetics Department, Hospital Universitario Central de Asturias, Oviedo, Spain.
Arq Bras Oftalmol ; 2023 Apr 03.
Article em En | MEDLINE | ID: mdl-37018821