Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome (Q77439740)
scientific article published on 01 March 1998
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| English | Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome |
scientific article published on 01 March 1998 |
Statements
Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome (English)
Denjoy I
Donger C
Gary F
Villain E
Leenhardt A
Benali K
Schwartz K
Coumel P