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Filters: Keyword is Polymorphism, Single-Stranded Conformational [Clear All Filters]
The distinct HERG missense mutation L564P causes long QT syndrome in one French Canadian family. Can J Cardiol. 2000;16(3):307-12.
Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes. Cardiovasc Res. 2000;46(1):55-65.