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Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene

Item Type:Article
Title:Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene
Creators Name:Weber, S. and Hoffmann, K. and Jeck, N. and Saar, K. and Boeswald, M. and Kuwertz-Broeking, E. and Meij, I.C. and Knoers, N.V.A.M. and Cochat, P. and Sulakova, T. and Bonzel, K.E. and Soergel, M. and Manz, F. and Schaerer, K. and Seyberth, H.W. and Reis, A. and Konrad, M.
Source:European Journal of Human Genetics
ISSN:1018-4813
Publisher:Nature Publishing Group (U.K.)
Volume:8
Page Range:414-422
Date:1 June 2000
Official Publication:http://www.nature.com/ejhg/journal/v8/n6/abs/5200475a.html
PubMed:View item in PubMed

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