Mutational screening of Indian families with hereditary congenital cataract

PURPOSE: To screen for pathogenic mutations in ten candidate genes in Indian families diagnosed with autosomal recessive and autosomal dominant cataracts. METHODS: Families with two or more affected individuals with bilateral familial congenital/developmental cataract were ophthalmically evaluated,...

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Detalles Bibliográficos
Autores principales: Ponnam, Surya Prakash Goud, Ramesha, Kekkunaya, Matalia, Jyoti, Tejwani, Sushma, Ramamurthy, Balasubramanya, Kannabiran, Chitra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669530/
https://www.ncbi.nlm.nih.gov/pubmed/23734083

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669530/
https://www.ncbi.nlm.nih.gov/pubmed/23734083

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