Referenced in: none

Automatically associated channels: Kv11.1 , Kv7.1

Title: A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family.

Authors: M J Ackerman, J J Schroeder, R Berry, D J Schaid, C J Porter, V V Michels, S N Thibodeau

Journal, date & volume: Pediatr. Res., 1998 Aug , 44, 148-53

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/9702906

Abstract