Molecular Strategies for RPGR Gene Therapy

Mutations affecting the Retinitis Pigmentosa GTPase Regulator (RPGR) gene are the commonest cause of X-linked and recessive retinitis pigmentosa (RP), accounting for 10%–20% of all cases of RP. The phenotype is one of the most severe amongst all causes of RP, characteristic for its early onset and r...

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Detalles Bibliográficos
Autores principales: Cehajic Kapetanovic, Jasmina, McClements, Michelle E, Martinez-Fernandez de la Camara, Cristina, MacLaren, Robert E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770968/
https://www.ncbi.nlm.nih.gov/pubmed/31487940
http://dx.doi.org/10.3390/genes10090674

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770968/
https://www.ncbi.nlm.nih.gov/pubmed/31487940
http://dx.doi.org/10.3390/genes10090674

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