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

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

DOI Full Paper Access

93

Citations

17

References

2000

Year

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

European Journal of Human Genetics

Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseNephrocalcinosis MapsPathologyMolecular GeneticsDisease Gene IdentificationFamilial HypomagnesaemiaMedicinePcln-1 GeneClinical Genetics

References

	Year	Citations

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