Referenced in: none

Automatically associated channels: Kir6.2

Title: Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia.

Authors: Roxanne Y Walder, Daniel Landau, Peter Meyer, Hanna Shalev, Maria Tsolia, Zvi Borochowitz, Melanie Barbara Boettger, Gretel E Beck, Richard K Englehardt, Rivka Carmi, Val C Sheffield

Journal, date & volume: Nat. Genet., 2002 Jun , 31, 171-4

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/12032570

Abstract