Truncating Mutation in theNHSGene: Phenotypic Heterogeneity of Nance-Horan Syndrome in an Asian Indian Family-Reference-Cited by-同舟云学术

Truncating Mutation in theNHSGene: Phenotypic Heterogeneity of Nance-Horan Syndrome in an Asian Indian Family

Published:2005-01-01 Issue:1 Volume:46 Page:17
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Ramprasad Vedam Lakshmi¹,Thool Alka²,Murugan Sakthivel¹,Nancarrow Derek³,Vyas Prateep²,Rao Srinivas Kamalakar⁴,Vidhya Authiappan¹,Ravishankar Krishnamoorthy⁴,Kumaramanickavel Govindasamy¹

Affiliation:

1. From the Department of Genetics and Molecular Biology, Vision Research Foundation, Sankara Nethralaya, Chennai, India; the

2. Shri Ganapati Nethralaya, Jalna, Maharashtra, India; the

3. Queensland Institute of Medical Research, Brisbane, Australia; the

4. Department of Cataract and IOL Implantation, Medical Research Foundation, Sankara Nethralaya, Chennai, India.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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