Homozygosity Mapping in Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa in South Indian Families

Leber congenital amaurosis (LCA) and retinitis pigmentosa (RP) are retinal degenerative diseases which cause severe retinal dystrophy affecting the photoreceptors. LCA is predominantly inherited as an autosomal recessive trait and contributes to 5% of all retinal dystrophies; whereas RP is inherited...

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Detalles Bibliográficos
Autores principales: Srilekha, Sundaramurthy, Arokiasamy, Tharigopala, Srikrupa, Natarajan N., Umashankar, Vetrivel, Meenakshi, Swaminathan, Sen, Parveen, Kapur, Suman, Soumittra, Nagasamy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493089/
https://www.ncbi.nlm.nih.gov/pubmed/26147992
http://dx.doi.org/10.1371/journal.pone.0131679

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493089/
https://www.ncbi.nlm.nih.gov/pubmed/26147992
http://dx.doi.org/10.1371/journal.pone.0131679

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