A founder deletion in the TRPM1 gene associated with congenital stationary night blindness and myopia is highly prevalent in Ashkenazi Jews

Congenital stationary night blindness (CSNB) is a disease affecting the night vision of individuals. Previous studies identified TRPM1 as a gene involved in reduced night vision. Homozygous deletion of TRPM1 was the cause of CSNB in several children in 6 Ashkenazi Jewish families, thereby prompting...

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Detalles Bibliográficos
Autores principales: Hirsch, Yoel, Zeevi, David A., Lam, Byron L., Scher, Sholem Y., Bringer, Rachel, Cherki, Bitya, Cohen, Cadina C., Muallem, Hagit, Chiang, John (Pei-Wen), Pantrangi, Madhulatha, Ekstein, Josef, Johansson, Martin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804618/
https://www.ncbi.nlm.nih.gov/pubmed/31645983
http://dx.doi.org/10.1038/s41439-019-0076-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804618/
https://www.ncbi.nlm.nih.gov/pubmed/31645983
http://dx.doi.org/10.1038/s41439-019-0076-4

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