心房颤动分子机制的研究现状(3)
Function Mutation in Familial Atrial Fibrillation[J]. Science，2003，299(5604):251.
[16] Loussouarn G，Baro I，Escande D.KCNQ1 K+ channel-mediated cardiac channelopathies[J].Methods Mol Biol，2006，337:167.
[17] Lai LP，Su MJ，Yeh HM，et al.Association of the human minK gene 38G allele with atrial fibrillation:evidence of possible genetic control on the pathogenesis of atrial fibrillation[J].Am Heart J,2002,144:485.
[18] Decher N，Uyguner O，Schere CR，et al.hKChIP2 is a functional mod-ifier of hKv4.3 potassium channels:cloning and expression of a shorthKChlP2 splice variant[J].Cardiovasc Res,2001,52:255.
[19] Hanson EL,Jakobs PM,Keegan H,et al.Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy[J].J Card Fail,2002, 8:28.
[20] Garg A,Speckman RA,Bowcock AM.Multisystem dystrophy syndromedue to novel missense mutations in the aminoterminal head and alp-ha-helical rod domains of the lamin A/C gene[J]. Am J Med，2002，112:549.
[21] Gollob MH,Seger JJ,Gollob TN,et al.Novel PRKAG2 mutation resp-onsible for the genetic syndrome of ventricular preexcitation and con-duction system disease with childhood onset and absence of cardiachypertrophy[J].Circulation,2001,104:3030.
[22] Ellinor PT,Shin JT,Moore RK,et al.Locus for atrial fibrillation maps to chromosome 6q14-16[J].Circulation,2003,107(23):2880.
[23] Temple J，Frias P，Rottman J，et al.Atrial fibrillation in KCNE1-nullmice[J].Circ Res，2005，97:62.
收稿日期：2007-03
[ 上 页 ], http://www.100md.com(郑文武 黄昌成 张晓刚)
[16] Loussouarn G，Baro I，Escande D.KCNQ1 K+ channel-mediated cardiac channelopathies[J].Methods Mol Biol，2006，337:167.
[17] Lai LP，Su MJ，Yeh HM，et al.Association of the human minK gene 38G allele with atrial fibrillation:evidence of possible genetic control on the pathogenesis of atrial fibrillation[J].Am Heart J,2002,144:485.
[18] Decher N，Uyguner O，Schere CR，et al.hKChIP2 is a functional mod-ifier of hKv4.3 potassium channels:cloning and expression of a shorthKChlP2 splice variant[J].Cardiovasc Res,2001,52:255.
[19] Hanson EL,Jakobs PM,Keegan H,et al.Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy[J].J Card Fail,2002, 8:28.
[20] Garg A,Speckman RA,Bowcock AM.Multisystem dystrophy syndromedue to novel missense mutations in the aminoterminal head and alp-ha-helical rod domains of the lamin A/C gene[J]. Am J Med，2002，112:549.
[21] Gollob MH,Seger JJ,Gollob TN,et al.Novel PRKAG2 mutation resp-onsible for the genetic syndrome of ventricular preexcitation and con-duction system disease with childhood onset and absence of cardiachypertrophy[J].Circulation,2001,104:3030.
[22] Ellinor PT,Shin JT,Moore RK,et al.Locus for atrial fibrillation maps to chromosome 6q14-16[J].Circulation,2003,107(23):2880.
[23] Temple J，Frias P，Rottman J，et al.Atrial fibrillation in KCNE1-nullmice[J].Circ Res，2005，97:62.
收稿日期：2007-03
[ 上 页 ], http://www.100md.com(郑文武 黄昌成 张晓刚)