Functional characterization of zebrafish orthologs of the human Beta 3-Glucosyltransferase B3GLCT gene mutated in Peters Plus Syndrome
Author:
Funder
National Eye Institute
National Institute of General Medical Sciences
Children's Hospital of Wisconsin
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference71 articles.
1. The Peters' plus syndrome: a review;LJ Maillette de Buy Wenniger-Prick;Ann Genet,2002
2. Mutation analysis of B3GALTL in Peters Plus syndrome;LM Reis;Am J Med Genet A,2008
3. Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes;E Weh;Clin Genet,2014
4. Anterior segment dysgenesis: Peters anomaly and sclerocornea;M Harissi-Dagher;Int Ophthalmol Clin,2008
5. Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferase;SA Lesnik Oberstein;Am J Hum Genet,2006
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