Mutation Analysis of Congenital Cataracts in Indian Families: Identification of SNPs and a New Causative Allele inCRYBB2Gene-Reference-Cited by-同舟云学术

Mutation Analysis of Congenital Cataracts in Indian Families: Identification of SNPs and a New Causative Allele inCRYBB2Gene

Published:2004-10-01 Issue:10 Volume:45 Page:3599
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Santhiya Sathiyavedu T.¹,Manisastry Shyam Manohar¹,Rawlley Deepika¹,Malathi Raghunathan¹,Anishetty Sharmila²,Gopinath Puthiya M.¹,Vijayalakshmi Perumalsamy³,Namperumalsamy Perumalsamy³,Adamski Jerzy⁴,Graw Jochen⁵

Affiliation:

1. From the Dr. ALM Postgraduate Institute of Basic Medical Sciences, Department of Genetics, University of Madras, Taramani, Chennai, India;

2. Center for BioTechnology, Anna University, Chennai, India;

3. Aravind Eye Hospital and Postgraduate Institute of Ophthalmology, Madurai, India; and Institutes of

4. Experimental and

5. Developmental Genetics, GSF-National Research Center for Environment and Health, Neuherberg, Germany.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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