Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction

Abstract Background Autosomal dominant polycystic kidney disease (ADPKD), the commonest inherited kidney disease, is generally caused by heterozygous mutations in PKD1, PKD2, or GANAB (PKD3). Methods We performed mutational analyses of PKD genes to identify causative mutations. A set of 90 unrelated...

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Автори:	Wen-Bin He, Wen-Juan Xiao, Yue-Qiu Tan, Xiao-Meng Zhao, Wen Li, Qian-Jun Zhang, Chang-Gao Zhong, Xiu-Rong Li, Liang Hu, Guang-Xiu Lu, Ge Lin, Juan Du
Формат:	Artigo
Мова:	Inglês
Опубліковано:	BMC 2018-10-01
Серія:	BMC Medical Genetics
Предмети:	Autosomal dominant polycystic kidney disease PKD1 gene PKD2 gene GANAB gene Novel mutation Male infertility
Онлайн доступ:	http://link.springer.com/article/10.1186/s12881-018-0693-7
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