Hypomagnesemia and nephrocalcinosis in a patient with two heterozygous mutations in the CLDN16 gene

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Spectral Karyotyping to Study Chromosome Abnormalities in Humans and Mice with Polycystic Kidney Disease
12:47

Spectral Karyotyping to Study Chromosome Abnormalities in Humans and Mice with Polycystic Kidney Disease

Published on: February 3, 2012

Katrin Staiger1, Harald Staiger, Carina Haas

  • 1Section of Nephrology and Hypertension, Division of Endocrinology, Department of Internal Medicine, Eberhard-Karls-University Tübingen, Tübingen - Germany. harald.staiger@med.uni-tuebingen.de

Journal of Nephrology
|March 10, 2007
PubMed

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