Novel mutations in CRYGD are associated with congenital cataracts in Chinese families

Congenital cataract disease is a clinically and genetically heterogeneous lens disorder. The purpose of this study was to identify the genetic defects and to investigate the relationships between disease-causing genes and lens morphology in congenital cataracts. Patients were given a physical examin...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Guoxing, Chen, Zhimin, Zhang, Wulin, Liu, Zhiqiang, Zhao, Jialiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702117/
https://www.ncbi.nlm.nih.gov/pubmed/26732753
http://dx.doi.org/10.1038/srep18912

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702117/
https://www.ncbi.nlm.nih.gov/pubmed/26732753
http://dx.doi.org/10.1038/srep18912

Ejemplares similares