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Mutations in TULP1, NR2E3, and MFRP genes in Indian families with autosomal recessive retinitis pigmentosa

PURPOSE: To identify genes underlying autosomal recessive retinitis pigmentosa (ARRP) by homozygosity mapping. METHODS: Families with ARRP were recruited after complete ophthalmic evaluation of all members and diagnosis of RP by predefined criteria. Genomic DNA from affected members of 26 families w...

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Detalles Bibliográficos
Autores principales:	Kannabiran, Chitra, Singh, Hardeep, Sahini, Nishika, Jalali, Subhadra, Mohan, Gayathri
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Molecular Vision 2012
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3351411/ https://www.ncbi.nlm.nih.gov/pubmed/22605927

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