Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.

Chen, Q; Zhang, D; Gingell, Rl; Moss, Aj; Napolitano, C; Priori, SILVIA GIULIANA; Schwartz, Peter; Kehoe, E; Robinson, Jl; Schulze Bahr, E; Wang, Q; Towbin, Ja