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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Mol Genet Genomic Med
Egile Nagusiak: Wang, Tao, Li, Qinggang, Shang, Shunlai, Geng, Guangrui, Xie, Yuansheng, Cai, Guangyan, Chen, Xiangmei
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: John Wiley and Sons Inc. 2019
Gaiak:
Original Articles
Sarrera elektronikoa: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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