Papers: 10.3390/genes12020171

https://doi.org/10.3390/genes12020171

A Novel Splice-Site Variant in CACNA1F Causes a Phenotype Synonymous with Åland Island Eye Disease and Incomplete Congenital Stationary Night Blindness

Cited by: 7
Author(s): Usman Mahmood, Cécile Méjécase, Syed S. Ali, Mariya Moosajee, Igor Kozák
Published: over 5 years ago

Software Mentions 1