Novel frameshift mutation in NYX...

Ophthalmic Genetics 2019 / 12

Novel frameshift mutation in NYX gene in a Russian family with complete congenital stationary night blindness

Ivanova, Marianna E., Zolnikova, Inna V., Gorgisheli, Ketevan V., Atarshchikov, Dmitry S., Ghosh, Preetam, Barh, Debmalya
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Journal:
Ophthalmic Genetics
DOI:
10.1080/13816810.2019.1698617
Date:
December, 2019
File:
PDF, 1.79 MB
2019
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