Read + Share
Amedeo Smart
Independent Medical Education
Mihalich A, Cammarata G, Tremolada G, Pollazzon M, et al. Two novel CACNA1F gene mutations cause two different phenotypes: Aland Eye Disease and incomplete Congenital Stationary Night Blindness. Exp Eye Res 2022;221:109143.PMID: 35697328
Email
LinkedIn
Facebook
Twitter
Privacy Policy