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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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發表在: | PLoS One |
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Main Authors: | , , , , , , , |
格式: | Artigo |
語言: | Inglês |
出版: |
Public Library of Science
2015
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主題: | |
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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