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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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Bibliografske podrobnosti
izdano v:Sci Rep
Main Authors: Jin, Meiling, Xie, Yuansheng, Chen, Zhiqiang, Liao, Yujie, Li, Zuoxiang, Hu, Panpan, Qi, Yan, Yin, Zhiwei, Li, Qinggang, Fu, Ping, Chen, Xiangmei
Format: Artigo
Jezik:Inglês
Izdano: Nature Publishing Group 2016
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5080601/
https://ncbi.nlm.nih.gov/pubmed/27782177
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep35945
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