Exploring the Variable Phenotypes of RPGR Carrier Females in Assessing Their Potential for Retinal Gene Therapy

Inherited retinal degenerations are the leading cause of blindness in the working population. X-linked retinitis pigmentosa (XLRP), caused by mutations in the Retinitis pigmentosa GTPase regulator (RPGR) gene is one of the more severe forms, and female carriers of RPGR mutations have a variable pres...

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Detalles Bibliográficos
Autores principales: Nanda, Anika, Salvetti, Anna P., Clouston, Penny, Downes, Susan M., MacLaren, Robert E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316369/
https://www.ncbi.nlm.nih.gov/pubmed/30567410
http://dx.doi.org/10.3390/genes9120643

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316369/
https://www.ncbi.nlm.nih.gov/pubmed/30567410
http://dx.doi.org/10.3390/genes9120643

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