A Novel Dominant Mutation in SAG, the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United States

PURPOSE: To identify the causes of autosomal dominant retinitis pigmentosa (adRP) in a cohort of families without mutations in known adRP genes and consequently to characterize a novel dominant-acting missense mutation in SAG. METHODS: Patients underwent ophthalmologic testing and were screened for...

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Detalles Bibliográficos
Autores principales: Sullivan, Lori S., Bowne, Sara J., Koboldt, Daniel C., Cadena, Elizabeth L., Heckenlively, John R., Branham, Kari E., Wheaton, Dianna H., Jones, Kaylie D., Ruiz, Richard S., Pennesi, Mark E., Yang, Paul, Davis-Boozer, David, Northrup, Hope, Gurevich, Vsevold V., Chen, Rui, Xu, Mingchu, Li, Yumei, Birch, David G., Daiger, Stephen P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2017
Materias:
Biochemistry and Molecular Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455168/
https://www.ncbi.nlm.nih.gov/pubmed/28549094
http://dx.doi.org/10.1167/iovs.16-21341

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455168/
https://www.ncbi.nlm.nih.gov/pubmed/28549094
http://dx.doi.org/10.1167/iovs.16-21341

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