Leahy, K.E.; Wright, T.; Grudzinska Pechhacker, M.K.; Audo, I.; Tumber, A.; Tavares, E.; MacDonald, H.; Locke, J.; VandenHoven, C.; Zeitz, C.;
et al. Optic Atrophy and Inner Retinal Thinning in CACNA1F-Related Congenital Stationary Night Blindness. Genes 2021, 12, 330.
https://doi.org/10.3390/genes12030330
AMA Style
Leahy KE, Wright T, Grudzinska Pechhacker MK, Audo I, Tumber A, Tavares E, MacDonald H, Locke J, VandenHoven C, Zeitz C,
et al. Optic Atrophy and Inner Retinal Thinning in CACNA1F-Related Congenital Stationary Night Blindness. Genes. 2021; 12(3):330.
https://doi.org/10.3390/genes12030330
Chicago/Turabian Style
Leahy, Kate E, Tom Wright, Monika K Grudzinska Pechhacker, Isabelle Audo, Anupreet Tumber, Erika Tavares, Heather MacDonald, Jeff Locke, Cynthia VandenHoven, Christina Zeitz,
and et al. 2021. "Optic Atrophy and Inner Retinal Thinning in CACNA1F-Related Congenital Stationary Night Blindness" Genes 12, no. 3: 330.
https://doi.org/10.3390/genes12030330
APA Style
Leahy, K. E., Wright, T., Grudzinska Pechhacker, M. K., Audo, I., Tumber, A., Tavares, E., MacDonald, H., Locke, J., VandenHoven, C., Zeitz, C., Heon, E., Buncic, J. R., & Vincent, A.
(2021). Optic Atrophy and Inner Retinal Thinning in CACNA1F-Related Congenital Stationary Night Blindness. Genes, 12(3), 330.
https://doi.org/10.3390/genes12030330