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Archives Des Maladies Du Coeur Et Des Vaisseaux|June 15, 1999
[Congenital long QT syndrome. The value of genetics in prognostic evaluation]I Denjoy, J M Lupoglazoff, C Donger, et al.Nature Genetics|February 1, 1997
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndromeN Neyroud, F Tesson, I Denjoy, et al.European Heart Journal|March 21, 1998
Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndromeN Neyroud, P Maison-Blanche, I Denjoy, et al.Circulation Research|February 19, 1999
Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndromeN Neyroud, P Richard, N Vignier, et al.Circulation|February 27, 2001
Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutationsJ M Lupoglazoff, I Denjoy, M Berthet, et al.Circulation|September 8, 1999
Splicing mutations in KCNQ1: a mutation hot spot at codon 344 that produces in frame transcriptsA Murray, C Donger, C Fenske, et al.Pageof 2