Referenced in: none

Automatically associated channels: Kir2.1

Title: Functional and clinical characterization of a mutation in KCNJ2 associated with Andersen-Tawil syndrome.

Authors: C-W Lu, J-H Lin, Y S Rajawat, H Jerng, T G Rami, X Sanchez, G DeFreitas, B Carabello, F DeMayo, D L Kearney, G Miller, H Li, P J Pfaffinger, N E Bowles, D S Khoury, J A Towbin

Journal, date & volume: J. Med. Genet., 2006 Aug , 43, 653-9

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/16571646

Abstract