CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis

Konrad, Martin; Hou, Jianghui; Weber, Stefanie; Dötsch, Jörg; Kari, Jameela A; Seeman, Tomas; Kuwertz-Bröking, Eberhard; Peco-Antic, Amira; Tasic, Velibor; Dittrich, Katalin; Alshaya, Hammad O; von Vigier, Rodo O; Gallati, Sabina; Goodenough, Daniel A; Schaller, André (2008). CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis. Journal of the American Society of Nephrology, 19(1), pp. 171-81. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1681/ASN.2007060709

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Item Type:	Journal Article (Original Article)
Division/Institute:	04 Faculty of Medicine > Department of Gynaecology, Paediatrics and Endocrinology (DFKE) > Clinic of Paediatric Medicine
UniBE Contributor:	Konrad, Martin, von Vigier, Rodo, Gallati, Sabina, Schaller, André
ISSN:	1046-6673
ISBN:	18003771
Publisher:	Lippincott Williams & Wilkins
Language:	English
Submitter:	Anette van Dorland
Date Deposited:	04 Oct 2013 14:55
Last Modified:	05 Dec 2022 14:17
Publisher DOI:	10.1681/ASN.2007060709
PubMed ID:	18003771
Web of Science ID:	000252293100024
URI:	https://boris.unibe.ch/id/eprint/23420 (FactScience: 41768)