PKD1 interacts with PKD2 through a probable coiled-coil domain

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) describes a group of at least three genetically distinct disorders with almost identical clinical features1–6 that collectively affects 1:1,000 of the population7. Affected individuals typically develop large cystic kidneys and approximately one half develop end-stage renal disease by their seventh decade… (More)
DOI: 10.1038/ng0697-179

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Cite this paper

@article{Qian1997PKD1IW, title={PKD1 interacts with PKD2 through a probable coiled-coil domain}, author={Feng Qian and F. Joseph Germino and Yiqiang Cai and Xiangbin Zhang and Stefan Somlo and Gregory G Germino}, journal={Nature Genetics}, year={1997}, volume={16}, pages={179-183} }