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 and Schaller, André

ISSN:

1046-6673

ISBN:

18003771

Publisher:

Lippincott Williams & Wilkins

Language:

English

Submitter:

Factscience Import

Date Deposited:

04 Oct 2013 14:55

Last Modified:

04 May 2014 23:16

Publisher DOI:

10.1681/ASN.2007060709

PubMed ID:

18003771

Web of Science ID:

000252293100024

URI:

https://boris.unibe.ch/id/eprint/23420 (FactScience: 41768)

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