共 50 条
- [26] KVLQT1, a polyvalent maestro implicated in Beckwith-Wiedemann syndrome. M S-MEDECINE SCIENCES, 1997, 13 (05): : 716 - 717
- [27] 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
- [30] Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome Human Genetics, 1998, 103 : 290 - 294