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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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書目詳細資料
發表在:PLoS One
Main Authors: Srilekha, Sundaramurthy, Arokiasamy, Tharigopala, Srikrupa, Natarajan N., Umashankar, Vetrivel, Meenakshi, Swaminathan, Sen, Parveen, Kapur, Suman, Soumittra, Nagasamy
格式: Artigo
語言:Inglês
出版: Public Library of Science 2015
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC4493089/
https://ncbi.nlm.nih.gov/pubmed/26147992
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0131679
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