Identifying gene mutations of Chinese patients with polycystic kidney disease through targeted next‐generation sequencing technology

BACKGROUND: Polycystic kidney disease (PKD) is the most common hereditary kidney disease. The main mutational genes causing autosomal dominant polycystic kidney disease (ADPKD) are PKD1 and PKD2 as well as some rare pathogenic genes. Unilateral PKD is rare in clinics, and its association with gene m...

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Vydáno v:Mol Genet Genomic Med
Hlavní autoři: Wang, Tao, Li, Qinggang, Shang, Shunlai, Geng, Guangrui, Xie, Yuansheng, Cai, Guangyan, Chen, Xiangmei
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2019
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Original Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6565597/
https://ncbi.nlm.nih.gov/pubmed/31056860
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.720
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