Referenced in: none

Automatically associated channels: Kir2.1

Title: A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen-Tawil syndrome.

Authors: Hoi-Fong Chan, Meng-Ling Chen, Jen-Jen Su, Li-Chin Ko, Chin-Hsien Lin, Ruey-Meei Wu

Journal, date & volume: J. Hum. Genet., 2010 Mar , 55, 186-8

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/20111058

Abstract