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

Congenital cataract (CC), responsible for about one-third of blindness in infants, is a major cause of vision loss in children worldwide. 10–25% of CC cases are attributed to genetic causes and CC is a clinically and genetically highly heterogeneous lens disorder in children. Autosomal dominant (AD)...

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Detalles Bibliográficos
Autores principales: Zhong, Zilin, Wu, Zehua, Han, Liyun, Chen, Jianjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428270/
https://www.ncbi.nlm.nih.gov/pubmed/28298635
http://dx.doi.org/10.1038/s41598-017-00318-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428270/
https://www.ncbi.nlm.nih.gov/pubmed/28298635
http://dx.doi.org/10.1038/s41598-017-00318-1

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