Identification of novel mutations in Chinese Hans with autosomal dominant polycystic kidney disease

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited renal disease with an incidence of 1 in 400 to 1000. The disease is genetically heterogeneous, with two genes identified: PKD1 (16p13.3) and PKD2 (4q21). Molecular diagnosis of the disease in at-risk indivi...

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Detalhes bibliográficos
Main Authors: Yu, Chaowen, Yang, Yuan, Zou, Lin, Hu, Zhangxue, Li, Jing, Liu, Yunqiang, Ma, Yongxin, Ma, Mingyi, Su, Dan, Zhang, Sizhong
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2011
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3341574/
https://ncbi.nlm.nih.gov/pubmed/22185115
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-12-164
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