Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia.
Walder, Roxanne Y
Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia. [electronic resource] - Nature genetics Jun 2002 - 171-4 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
1061-4036
10.1038/ng901 doi
DNA Mutational Analysis
Humans
Hypocalcemia--etiology
Ion Channels--genetics
Magnesium--blood
Molecular Sequence Data
Mutation
Pedigree
Sequence Analysis, DNA
TRPM Cation Channels
Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia. [electronic resource] - Nature genetics Jun 2002 - 171-4 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
1061-4036
10.1038/ng901 doi
DNA Mutational Analysis
Humans
Hypocalcemia--etiology
Ion Channels--genetics
Magnesium--blood
Molecular Sequence Data
Mutation
Pedigree
Sequence Analysis, DNA
TRPM Cation Channels