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Neyroud Nathalie
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Sorbonne Université - Paris / France
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Neyroud Nathalie's MOST POPULAR ARTICLES
1-)
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome N Neyroud, F Tesson, I Denjoy, M Leibovici, C Donger, J Barhanin, ... Nature genetics 15 (2), 186-189, 1997 10371997
2-)
KVLQT1 C-Terminal Missense Mutation Causes a Forme Fruste Long-QT Syndrome C Donger, I Denjoy, M Berthet, N Neyroud, C Cruaud, M Bennaceur, ... Circulation 96 (9), 2778-2781, 1997 4691997
3-)
Properties of KvLQT1 K+ channel mutations in Romano–Ward and Jervell and Lange‐Nielsen inherited cardiac arrhythmias C Chouabe, N Neyroud, P Guicheney, M Lazdunski, G Romey, ... The EMBO Journal 16 (17), 5472-5479, 1997 3391997
4-)
MOG1 A New Susceptibility Gene for Brugada SyndromeD Kattygnarath, S Maugenre, N Neyroud, E Balse, C Ichai, I Denjoy, ...Circulation: Cardiovascular Genetics 4 (3), 261-268, 20111952011
5-)
Isoform-Specific Modulation of Voltage-Gated Na+ Channels by CalmodulinI Deschênes, N Neyroud, D DiSilvestre, E Marbán, DT Yue, ...Circulation research 90 (4), e49-e57, 20021892002
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