Familial hypomagnesemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN1-gene.

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Publication year
2000
Author(s)
Weber, S.
Hoffmann, K.
Jeck, N.
Saar, K.
Boeswald, M.
Kuwertz-Broeking, E.
Meij, I.C.
Knoers, N.V.A.M.
Cochat, P.
Sulakova, T.
Bonzel, K.E.
Soergel, M.
Manz, F.
Schaerer, K.
Seyberth, H.W.
Reis, A.
Konrad, M.
Number of pages
9 p.
Source
European Journal of Human Genetics, 8, 6, (2000), pp. 414-422
ISSN
DOI
Publication type
Article / Letter to editor
If a DOI or any other persistent identifier is unavailable, please use the following repository identifier to link to this item: https://hdl.handle.net/2066/184486   https://hdl.handle.net/2066/184486
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