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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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Main Authors: Devi, Ramachandran Ramya, Yao, Wenliang, Vijayalakshmi, Perumalsamy, Sergeev, Yuri V., Sundaresan, Periasamy, Hejtmancik, J. Fielding
Format: Artigo
Sprog:Inglês
Udgivet: Molecular Vision 2008
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Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2435160/
https://ncbi.nlm.nih.gov/pubmed/18587492
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