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

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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:	Weber, S., Hoffmann, K., Jeck, N., Saar, K. ORCID: https://orcid.org/0000-0002-4483-1557, Boeswald, M., Kuwertz-Broeking, E., Meij, I.C. ORCID: https://orcid.org/0000-0002-8189-2762, Knoers, N.V.A.M., Cochat, P., Sulakova, T., Bonzel, K.E., Soergel, M., Manz, F., Schaerer, K., Seyberth, H.W., Reis, A. and Konrad, M.
Source:	European Journal of Human Genetics
ISSN:	1018-4813
Publisher:	Nature Publishing Group
Volume:	8
Page Range:	414-422
Date:	1 June 2000
Official Publication:	https://doi.org/10.1038/sj.ejhg.5200475
PubMed:	View item in PubMed

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