Retinitis pigmentosa: mutation analysis of RHO, PRPF31, RP1, and IMPDH1 genes in patients from India

PURPOSE: To screen for possible disease-causing mutations in rhodopsin (RHO), pre-mRNA processing factor 31 (PRPF31), retinitis pigmentosa 1 (RP1), and inosine monophosphate dehydrogenase 1 (IMPDH1) genes in Indian patients with isolated and autosomal dominant forms of retinitis pigmentosa (adRP). I...

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Detalles Bibliográficos
Autores principales: Gandra, Mamatha, Anandula, Venkataramana, Authiappan, Vidhya, Sundaramurthy, Srilekha, Raman, Rajiv, Bhattacharya, Shomi, Govindasamy, Kumaramanickavel
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426732/
https://www.ncbi.nlm.nih.gov/pubmed/18552984

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426732/
https://www.ncbi.nlm.nih.gov/pubmed/18552984

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