Novel crystallin gamma B mutations in a Kuwaiti family with autosomal dominant congenital cataracts reveal genetic and clinical heterogeneity

Novel crystallin gamma B mutations in a Kuwaiti family with autosomal dominant congenital cataracts reveal genetic and clinical heterogeneity

Bibliographic Details
Main Authors: AlFadhli, Suad, Abdelmoaty, Sidky, Al-Hajeri, Amal, Behbehani, Abdulmutalib, Alkuraya, Fowzan
Format: Online
Language:English
Published: Molecular Vision 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533929/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533929/

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