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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Detaylı Bibliyografya
Yayımlandı:Mol Genet Genomic Med
Asıl Yazarlar: Wang, Tao, Li, Qinggang, Shang, Shunlai, Geng, Guangrui, Xie, Yuansheng, Cai, Guangyan, Chen, Xiangmei
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2019
Konular:
Original Articles
Online Erişim: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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