Mahmood, U.; Méjécase, C.; Ali, S.M.A.; Moosajee, M.; Kozak, I.
A Novel Splice-Site Variant in CACNA1F Causes a Phenotype Synonymous with Åland Island Eye Disease and Incomplete Congenital Stationary Night Blindness. Genes 2021, 12, 171.
https://doi.org/10.3390/genes12020171
AMA Style
Mahmood U, Méjécase C, Ali SMA, Moosajee M, Kozak I.
A Novel Splice-Site Variant in CACNA1F Causes a Phenotype Synonymous with Åland Island Eye Disease and Incomplete Congenital Stationary Night Blindness. Genes. 2021; 12(2):171.
https://doi.org/10.3390/genes12020171
Chicago/Turabian Style
Mahmood, Usman, Cécile Méjécase, Syed M. A. Ali, Mariya Moosajee, and Igor Kozak.
2021. "A Novel Splice-Site Variant in CACNA1F Causes a Phenotype Synonymous with Åland Island Eye Disease and Incomplete Congenital Stationary Night Blindness" Genes 12, no. 2: 171.
https://doi.org/10.3390/genes12020171
APA Style
Mahmood, U., Méjécase, C., Ali, S. M. A., Moosajee, M., & Kozak, I.
(2021). A Novel Splice-Site Variant in CACNA1F Causes a Phenotype Synonymous with Åland Island Eye Disease and Incomplete Congenital Stationary Night Blindness. Genes, 12(2), 171.
https://doi.org/10.3390/genes12020171
