System analysis of gene mutations and clinical phenotype in Chinese patients with autosomal-dominant polycystic kidney disease

Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disorder mainly caused by mutation in PKD1/PKD2. However, ethnic differences in mutations, the association between mutation genotype/clinical phenotype, and the clinical applicable value of mutation detection ar...

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Detalles Bibliográficos
Autores principales: Jin, Meiling, Xie, Yuansheng, Chen, Zhiqiang, Liao, Yujie, Li, Zuoxiang, Hu, Panpan, Qi, Yan, Yin, Zhiwei, Li, Qinggang, Fu, Ping, Chen, Xiangmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5080601/
https://www.ncbi.nlm.nih.gov/pubmed/27782177
http://dx.doi.org/10.1038/srep35945

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5080601/
https://www.ncbi.nlm.nih.gov/pubmed/27782177
http://dx.doi.org/10.1038/srep35945

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