Bioinformatics analysis of CYP1B1 mutation hotspots in Chinese primary congenital glaucoma patients

Primary congenital glaucoma (PCG) is an inherited blinding eye disease. The CYP1B1 gene was identified as a causal gene for PCG, and many mutations have been found, but no studies have focussed on the molecular epidemiology of CYP1B1 in Chinese populations. We aimed to explore the CYP1B1 mutation ho...

Descripción completa

Detalles Bibliográficos
Autores principales: Ou, Zhiying, Liu, Guangjian, Liu, Wenping, Deng, Yehua, Zheng, Ling, Zhang, Shu, Feng, Guangqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2018
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435531/
https://www.ncbi.nlm.nih.gov/pubmed/29903728
http://dx.doi.org/10.1042/BSR20180056

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435531/
https://www.ncbi.nlm.nih.gov/pubmed/29903728
http://dx.doi.org/10.1042/BSR20180056

Ejemplares similares