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

    Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene 由 Stefanie Weber, Katrin Hoffmann, Nikola Jeck, Kathrin Saar, Martin Boeswald, Eberhard Kuwertz-Broeking, Ivan IC Meij, Nine Knoers, Pierre Cochat, Tereza Šuláková, Klaus E. Bonzel, Marianne Soergel, Friedrich Manz, K Schaerer, Hannsjoerg W. Seyberth, André Reis, Martin Konrad

    出版 2000
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