Novel TRPM6 Mutations in 21 Families with Primary Hypomagnesemia and Secondary Hypocalcemia-Reference-Cited by-同舟云学术

Novel TRPM6 Mutations in 21 Families with Primary Hypomagnesemia and Secondary Hypocalcemia

Published:2005-08-17 Issue:10 Volume:16 Page:3061-3069
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Schlingmann Karl P.,Sassen Martin C.,Weber Stefanie,Pechmann Ulla,Kusch Kerstin,Pelken Lutz,Lotan Daniel,Syrrou Maria,Prebble Jeffrey J.,Cole David E.C.,Metzger Daniel L.,Rahman Shamima,Tajima Toshihiro,Shu San-Ging,Waldegger Siegfried,Seyberth Hannsjoerg W.,Konrad Martin

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

Reference31 articles.

1. Evidence for Parathyroid Failure in Magnesium Deficiency

2. Primary hypomagnesemia

3. Studies in primary hypomagnesaemia: evidence for defective carrier-mediated small intestinal transport of magnesium.

4. Familial Hypomagnesemia—A Follow-Up Examination of Three Patients After 9 to 12 Years of Treatment

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