The EPHA2 gene is associated with cataracts linked to chromosome 1p

PURPOSE: Cataracts are a clinically and genetically heterogeneous disorder affecting the ocular lens, and the leading cause of treatable vision loss and blindness worldwide. Here we identify a novel gene linked with a rare autosomal dominant form of childhood cataracts segregating in a four generati...

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Detalles Bibliográficos
Autores principales: Shiels, Alan, Bennett, Thomas M., Knopf, Harry L.S., Maraini, Giovanni, Li, Anren, Jiao, Xiaodong, Hejtmancik, J. Fielding
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2582197/
https://www.ncbi.nlm.nih.gov/pubmed/19005574

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2582197/
https://www.ncbi.nlm.nih.gov/pubmed/19005574

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