Crystallin gene mutations in Indian families with inherited pediatric cataract

PURPOSE: Pediatric cataract is the most common form of treatable childhood blindness and is both clinically and genetically heterogeneous. Autosomal dominant and recessive forms of cataract have been reported to be caused by mutations in 22 different genes so far. Of the cataract mutations reported...

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Hlavní autoři: Devi, Ramachandran Ramya, Yao, Wenliang, Vijayalakshmi, Perumalsamy, Sergeev, Yuri V., Sundaresan, Periasamy, Hejtmancik, J. Fielding
Médium: Artigo
Jazyk:Inglês
Vydáno: Molecular Vision 2008
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2435160/
https://ncbi.nlm.nih.gov/pubmed/18587492
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