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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Опубликовано в: :PLoS One
Главные авторы: Srilekha, Sundaramurthy, Arokiasamy, Tharigopala, Srikrupa, Natarajan N., Umashankar, Vetrivel, Meenakshi, Swaminathan, Sen, Parveen, Kapur, Suman, Soumittra, Nagasamy
Формат: Artigo
Язык:Inglês
Опубликовано: Public Library of Science 2015
Предметы:
Research Article
Online-ссылка: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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