Optic Atrophy and Inner Retinal Thinning in CACNA1F-related Congenital Stationary Night Blindness.
Leahy KE, Wright T, Grudzinska Pechhacker MK, Audo I, Tumber A, Tavares E, MacDonald H, Locke J, VandenHoven C, Zeitz C, Heon E, Buncic JR, Vincent A.
Leahy KE, et al. Among authors: vandenhoven c.
Genes (Basel). 2021 Feb 25;12(3):330. doi: 10.3390/genes12030330.
Genes (Basel). 2021.
PMID: 33668843
Free PMC article.