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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Detalles Bibliográficos
Autores principales: Devi, Ramachandran Ramya, Yao, Wenliang, Vijayalakshmi, Perumalsamy, Sergeev, Yuri V., Sundaresan, Periasamy, Hejtmancik, J. Fielding
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2435160/
https://www.ncbi.nlm.nih.gov/pubmed/18587492

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2435160/
https://www.ncbi.nlm.nih.gov/pubmed/18587492

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