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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Autores principales: 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
Formato: Artigo
Lenguaje:Inglês
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea: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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