先天性长QT综合征的分子遗传学研究进展

Advances in Molecular Genetics Research of Congenital Long QT Syndrome

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作者王娟徐文渊陈义汉

机构地区同济大学附属同济医院心内科

出处《同济大学学报（医学版）》 CAS 2002年第1期54-58,共5页 Journal of Tongji University(Medical Science)

基金教育部青年骨干教师基金资助项目 ( 15 0 8-110 0 0 1)

关键词先天性长QT综合征离子通道心律失常分子遗传学研究进展

参考文献15

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6[6]Splawski I,Shen J,Timothy KW,et al.Spectrum of mutatio ns in long QT syndrome genes KVLQT1,HERG,SCN5A,KCNE1,and KCNE2[J].Circulation ,2000 ,102(10):1178-1185.
7[7]Jiang C,Atkinson D,Towbin JA,et al.Tow long QT syndrom loci map to chromosomes 3 and 7 with evidence for further heterogeneity[J].Na t Genet,1994,8:141-147.
8[8]Abbott GW,Sesti F,Splawski I,et al.MiRP1 forms IKr pot assium channels with HERG and is associated with cardiac arrhythmia[J].Cell, 1999,97(2):175-187.
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同济大学学报（医学版）

2002年第1期

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