Mutation of Solute Carrier SLC16A12 Associates with a Syndrome Combining Juvenile Cataract with Microcornea and Renal Glucosuria-Reference-Cited by-同舟云学术

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Mutation of Solute Carrier SLC16A12 Associates with a Syndrome Combining Juvenile Cataract with Microcornea and Renal Glucosuria

Published:2008-03 Issue:3 Volume:82 Page:772-779
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Kloeckener-Gruissem Barbara,Vandekerckhove Kristof,Nürnberg Gudrun,Neidhardt John,Zeitz Christina,Nürnberg Peter,Schipper Isaak,Berger Wolfgang

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference23 articles.

1. Growth of the human eye lens;Augusteyn;Mol. Vis.,2007

2. The genetics of childhood cataract;Francis;J. Med. Genet.,2000

3. Characterization of a familial t(16;22) balanced translocation associated with congenital cataract leads to identification of a novel gene, TMEM114, expressed in the lens and disrupted by the translocation;Jamieson;Hum. Mutat.,2007

4. Genetic examination in cases of congenital cataract;Lorenz;Ophthalmologe,2007

5. Genetic origins of cataract;Shiels;Arch. Ophthalmol.,2007

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