Search Page
Save citations to file
Email citations
Email address has not been verified. Go to
My NCBI account settings
to confirm your email and then refresh this page.
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
4 results
Filters applied: . Clear all
Page 1
Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia.
Nat Genet. 2002 Jun;31(2):171-4. doi: 10.1038/ng901. Epub 2002 May 28.
Nat Genet. 2002.
PMID: 12032570
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.
Schlingmann KP, Weber S, Peters M, Niemann Nejsum L, Vitzthum H, Klingel K, Kratz M, Haddad E, Ristoff E, Dinour D, Syrrou M, Nielsen S, Sassen M, Waldegger S, Seyberth HW, Konrad M.
Schlingmann KP, et al.
Nat Genet. 2002 Jun;31(2):166-70. doi: 10.1038/ng889. Epub 2002 May 28.
Nat Genet. 2002.
PMID: 12032568
Item in Clipboard
Mg2+ transport in the kidney.
Satoh J, Romero MF.
Satoh J, et al.
Biometals. 2002 Sep;15(3):285-95. doi: 10.1023/a:1016087017676.
Biometals. 2002.
PMID: 12206394
Review.
Item in Clipboard
Genetic disorders of magnesium homeostasis.
Meij IC, van den Heuvel LP, Knoers NV.
Meij IC, et al.
Biometals. 2002 Sep;15(3):297-307. doi: 10.1023/a:1016039101747.
Biometals. 2002.
PMID: 12206395
Review.
No abstract available.
Item in Clipboard
Cite
Cite
ARTICLE TYPE
ARTICLE LANGUAGE
AGE
Filters on the sidebar will be reset to the default list and any currently applied filters will be cleared.