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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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Detalhes bibliográficos
Main Authors: Ponnam, Surya Prakash Goud, Ramesha, Kekkunaya, Matalia, Jyoti, Tejwani, Sushma, Ramamurthy, Balasubramanya, Kannabiran, Chitra
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3669530/
https://ncbi.nlm.nih.gov/pubmed/23734083
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