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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Detalles Bibliográficos
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: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3754966/
https://www.ncbi.nlm.nih.gov/pubmed/24014202
http://dx.doi.org/10.1371/journal.pone.0072518

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3754966/
https://www.ncbi.nlm.nih.gov/pubmed/24014202
http://dx.doi.org/10.1371/journal.pone.0072518

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