Mutations in the EPHA2 Gene Are a Major Contributor to Inherited Cataracts in South-Eastern Australia

Congenital cataract is the most common cause of treatable visual impairment in children worldwide. Mutations in many different genes lead to congenital cataract. Recently, mutations in the receptor tyrosine kinase gene, EPHA2, have been found to cause congenital cataract in six different families. A...

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Main Authors: Dave, Alpana, Laurie, Kate, Staffieri, Sandra E., Taranath, Deepa, Mackey, David A., Mitchell, Paul, Wang, Jie Jin, Craig, Jamie E., Burdon, Kathryn P., Sharma, Shiwani
פורמט: Artigo
שפה:Inglês
יצא לאור: Public Library of Science 2013
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Research Article
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC3754966/
https://ncbi.nlm.nih.gov/pubmed/24014202
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0072518
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