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- [34] Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome European Journal of Human Genetics, 1998, 6 : 129 - 133
- [40] A Novel Mutation in KVLQT1 Is the Molecular Basis of Inherited Long QT Syndrome in a Near-Drowning Patient's Family Pediatric Research, 1998, 44 : 148 - 153