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27. PKD2-Related Autosomal Dominant Polycystic Kidney Disease: Prevalence, Clinical Presentation, Mutation Spectrum, and Prognosis. Cornec-Le Gall E; Audrézet MP; Renaudineau E; Hourmant M; Charasse C; Michez E; Frouget T; Vigneau C; Dantal J; Siohan P; Longuet H; Gatault P; Ecotière L; Bridoux F; Mandart L; Hanrotel-Saliou C; Stanescu C; Depraetre P; Gie S; Massad M; Kersalé A; Séret G; Augusto JF; Saliou P; Maestri S; Chen JM; Harris PC; Férec C; Le Meur Y Am J Kidney Dis; 2017 Oct; 70(4):476-485. PubMed ID: 28356211 [TBL] [Abstract][Full Text] [Related]
28. The Uromodulin C744G mutation causes MCKD2 and FJHN in children and adults and may be due to a possible founder effect. Wolf MT; Beck BB; Zaucke F; Kunze A; Misselwitz J; Ruley J; Ronda T; Fischer A; Eifinger F; Licht C; Otto E; Hoppe B; Hildebrandt F Kidney Int; 2007 Mar; 71(6):574-81. PubMed ID: 17245395 [TBL] [Abstract][Full Text] [Related]