A Novel MIP Gene Mutation Analysis in a Chinese Family Affected with Congenital Progressive Punctate Cataract

Congenital cataracts are one of the leading causes of visual impairment and blindness in children, and genetic factors play an important role in their development. This study aimed to identify the genetic defects associated with autosomal dominant congenital progressive punctate cataracts in a Chine...

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Detalles Bibliográficos
Autores principales: Ding, Xuchen, Zhou, Nan, Lin, Hui, Chen, Jianjun, Zhao, Chunyuan, Zhou, Guangkai, Hejtmancik, J. Fielding, Qi, Yanhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102541/
https://www.ncbi.nlm.nih.gov/pubmed/25033405
http://dx.doi.org/10.1371/journal.pone.0102733

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102541/
https://www.ncbi.nlm.nih.gov/pubmed/25033405
http://dx.doi.org/10.1371/journal.pone.0102733

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