(Q50998620)
Statements
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A mutation in HERG associated with notched T waves in long QT syndrome. (English)
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Dausse E
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Berthet M
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Denjoy I
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André-Fouet X
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Cruaud C
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Bennaceur M
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Fauré S
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Coumel P
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Schwartz K
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1 August 1996
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28
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8
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1609-1615
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Identifiers
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