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

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 famili...

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Detalles Bibliográficos
Autores principales: He, Wen-Bin, Xiao, Wen-Juan, Tan, Yue-Qiu, Zhao, Xiao-Meng, Li, Wen, Zhang, Qian-Jun, Zhong, Chang-Gao, Li, Xiu-Rong, Hu, Liang, Lu, Guang-Xiu, Lin, Ge, Du, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192368/
https://www.ncbi.nlm.nih.gov/pubmed/30333007
http://dx.doi.org/10.1186/s12881-018-0693-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192368/
https://www.ncbi.nlm.nih.gov/pubmed/30333007
http://dx.doi.org/10.1186/s12881-018-0693-7

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