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

✍ Scribed by Weber, Stefanie; Hoffmann, Katrin; Jeck, Nikola; Saar, Kathrin; Boeswald, Martin; Kuwertz-Broeking, Eberhard; Meij, Ivan IC; Knoers, Nine VAM; Cochat, Pierre; Šuláková, Tereza

Book ID: 110024969
Publisher: Nature Publishing Group
Year: 2000
Tongue: English
Weight: 234 KB
Volume: 8
Category: Article
ISSN: 1018-4813
DOI: 10.1038/sj.ejhg.5200475

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