학술논문
A novel phenotype in a family with autosomal dominant retinal dystrophy due to c.1430A > G in retinoid isomerohydrolase (RPE65) and c.37C > T in bestrophin 1 (BEST1)
Document Type
Article
Author
Source
In: Documenta Ophthalmologica . (Documenta Ophthalmologica, August 2021, 143(1):61-73)
Subject
Language
English
ISSN
15732622
00124486
00124486