LRP5 variants may contribute to ADPKD
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/ejhg201586.pdf
Reference33 articles.
1. Torres VE, Harris PC, Pirson Y : Autosomal dominant polycystic kidney disease. Lancet 2007; 369: 1287–1301.
2. Bae KT, Zhu F, Chapman AB et al: Magnetic resonance imaging evaluation of hepatic cysts in early autosomal-dominant polycystic kidney disease: the Consortium for Radiologic Imaging Studies of Polycystic Kidney Disease cohort. Clin J Am Soc Nephrol 2006; 1: 64–69.
3. Luciano RL, Dahl NK : Extra-renal manifestations of autosomal dominant polycystic kidney disease (ADPKD): considerations for routine screening and management. Nephrol Dial Transplant 2014; 29: 247–254.
4. Torra R, Darnell A, Estivill X et al: Interfamilial and intrafamilial variability of clinical expression in ADPKD. Contrib Nephrol 1995; 115: 97–101.
5. Liu M, Shi S, Senthilnathan S, Yu et al: Genetic variation of DKK3 may modify renal disease severity in ADPKD. J Am Soc Nephrol 2010; 21: 1510–1520.
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