Mutation Analysis of Congenital Cataracts in Indian Families: Identification of SNPs and a New Causative Allele inCRYBB2Gene
Investigative Ophthalmology & Visual Science2004Vol. 45(10), pp. 3599–3599
Citations Over TimeTop 21% of 2004 papers
Sathiyavedu Thyagarajan Santhiya, Shyam Manohar Manisastry, Deepika Rawlley, R. Malathi, Sharmila Anishetty, Puthiya M. Gopinath, P Vijayalakshmi, Perumalsamy Namperumalsamy, Jerzy Adamski, Jochen Graw
Abstract
Exon 6 of CRYBB2 appears to be a critical region susceptible for mutations leading to lens opacity.
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