Assessment of PAX6 alleles in 66 families with aniridia-Reference-Cited by-同舟云学术

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Assessment of PAX6 alleles in 66 families with aniridia

Published:2016-01-25 Issue:6 Volume:89 Page:669-677
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Bobilev A.M.¹,McDougal M.E.²,Taylor W.L.³,Geisert E.E.⁴,Netland P.A.³,Lauderdale J.D.¹²

Affiliation:

1. Neuroscience Division of the Biomedical and Health Sciences Institute; The University of Georgia; Athens GA USA

2. Department of Cellular Biology; The University of Georgia; Athens GA USA

3. Molecular Resource Center; The University of Tennessee Health Science Center; Memphis TN USA

4. Department of Ophthalmology in the Hamilton Eye Institute; The University of Tennessee Health Science Center; Memphis TN USA

Funder

National Institutes of Health

Research to Prevent Blindness

Hamilton Eye Institute

Sharon Stewart Aniridia Research Trust

Glaucoma Foundation

Vision for Tomorrow

Department of Cellular Biology Vision Research

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference76 articles.

1. PAX6 mutations in aniridia;Hanson;Hum Mol Genet,1993

2. Artificial iris-lens diaphragm in reconstructive surgery for aniridia and aphakia;Pozdeyeva;J Cataract Refract Surg,2005

3. Progressive changes in the angle in congenital aniridia, with development of glaucoma;Grant;Am J Ophthalmol,1974

4. Aniridia and optic nerve hypoplasia;McCulley;Eye (Lond),2005

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