A carregar...

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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Biosci Rep
Main Authors: Ou, Zhiying, Liu, Guangjian, Liu, Wenping, Deng, Yehua, Zheng, Ling, Zhang, Shu, Feng, Guangqiang
Formato: Artigo
Idioma:Inglês
Publicado em: Portland Press Ltd. 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6435531/
https://ncbi.nlm.nih.gov/pubmed/29903728
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BSR20180056
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!