Dominant Renin Gene Mutations Associated with Early-Onset Hyperuricemia, Anemia, and Chronic Kidney Failure-Reference-Cited by-同舟云学术

Dominant Renin Gene Mutations Associated with Early-Onset Hyperuricemia, Anemia, and Chronic Kidney Failure

Published:2009-08 Issue:2 Volume:85 Page:204-213
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Živná Martina,Hůlková Helena,Matignon Marie,Hodaňová Kateřina,Vylet'al Petr,Kalbáčová Marie,Barešová Veronika,Sikora Jakub,Blažková Hana,Živný Jan,Ivánek Robert,Stránecký Viktor,Sovová Jana,Claes Kathleen,Lerut Evelyne,Fryns Jean-Pierre,Hart P. Suzanne,Hart Thomas C.,Adams Jeremy N.,Pawtowski Audrey,Clemessy Maud,Gasc Jean-Marie,Gübler Marie-Claire,Antignac Corinne,Elleder Milan,Kapp Katja,Grimbert Philippe,Bleyer Anthony J.,Kmoch Stanislav

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference36 articles.

1. Genetic polymorphisms of the RAS-cytokine pathway and chronic kidney disease;Wong;Pediatr. Nephrol.,2008

2. Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis;Gribouval;Nat. Genet.,2005

3. A mutant renin gene in familial elevation of prorenin;Villard;J. Biol. Chem.,1994

4. Cloning and sequence analysis of cDNA for human renin precursor;Imai;Proc. Natl. Acad. Sci. USA,1983

5. Physiology of local renin-angiotensin systems;Paul;Physiol. Rev.,2006

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