A functional variant in NEPH3 gene confers high risk of renal failure in primary hematuric glomerulopathies. Evidence for predisposition to microalbuminuria in the general population-Reference-Cited by-同舟云学术

A functional variant in NEPH3 gene confers high risk of renal failure in primary hematuric glomerulopathies. Evidence for predisposition to microalbuminuria in the general population

Published:2017-03-23 Issue:3 Volume:12 Page:e0174274
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Voskarides Konstantinos,Stefanou Charalambos,Pieri Myrtani,Demosthenous Panayiota,Felekkis Kyriakos,Arsali Maria,Athanasiou Yiannis,Xydakis Dimitris,Stylianou Kostas,Daphnis Eugenios,Goulielmos Giorgos,Loizou Petros,Savige Judith,Höhne Martin,Völker Linus A.,Benzing Thomas,Maxwell Patrick H.,Gale Daniel P.,Gorski Mathias,Böger Carsten,Kollerits Barbara,Kronenberg Florian,Paulweber Bernhard,Zavros Michalis,Pierides Alkis,Deltas Constantinos

Funder

Cyprus Research Promotion Foundation

University of Cyprus

Else Kröner-Fresenius-Stiftung

Paracelsus Medical University Salzburg

"Genomics of Lipid associated Disorders – GOLD" of the "Austrian Genome Research Programme GEN-AU" and the Austrian Heart Fund

National Heart, Lung, and Blood Institute (NHLBI) in collaboration with Boston University

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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