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