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PUBMED FOR HANDHELDS

Journal Abstract Search


260 related items for PubMed ID: 10737999

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  • 2. Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.
    Larsen LA, Fosdal I, Andersen PS, Kanters JK, Vuust J, Wettrell G, Christiansen M.
    Eur J Hum Genet; 1999 Sep; 7(6):724-8. PubMed ID: 10482963
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  • 6. Dominant-negative I(Ks) suppression by KCNQ1-deltaF339 potassium channels linked to Romano-Ward syndrome.
    Thomas D, Wimmer AB, Karle CA, Licka M, Alter M, Khalil M, Ulmer HE, Kathöfer S, Kiehn J, Katus HA, Schoels W, Koenen M, Zehelein J.
    Cardiovasc Res; 2005 Aug 15; 67(3):487-97. PubMed ID: 15950200
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  • 7. Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.
    Chen Q, Zhang D, Gingell RL, Moss AJ, Napolitano C, Priori SG, Schwartz PJ, Kehoe E, Robinson JL, Schulze-Bahr E, Wang Q, Towbin JA.
    Circulation; 1999 Mar 16; 99(10):1344-7. PubMed ID: 10077519
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  • 9. KCNQ1 gene mutations and the respective genotype-phenotype correlations in the long QT syndrome.
    Herbert E, Trusz-Gluza M, Moric E, Smiłowska-Dzielicka E, Mazurek U, Wilczok T.
    Med Sci Monit; 2002 Oct 16; 8(10):RA240-8. PubMed ID: 12388934
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  • 14. Characterization and subcellular localization of KCNQ1 with a heterozygous mutation in the C terminus.
    Yamashita F, Horie M, Kubota T, Yoshida H, Yumoto Y, Kobori A, Ninomiya T, Kono Y, Haruna T, Tsuji K, Washizuka T, Takano M, Otani H, Sasayama S, Aizawa Y.
    J Mol Cell Cardiol; 2001 Feb 16; 33(2):197-207. PubMed ID: 11162126
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  • 16. [The mutation scanning of KCNQ1 gene for 31 long QT syndrome families].
    Li P, Li CL, Hu DY, Liu WL, Qin XG, Li YT, Li ZM, Li L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Jun 16; 21(3):236-9. PubMed ID: 15192825
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  • 20. Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.
    Jongbloed RJ, Wilde AA, Geelen JL, Doevendans P, Schaap C, Van Langen I, van Tintelen JP, Cobben JM, Beaufort-Krol GC, Geraedts JP, Smeets HJ.
    Hum Mutat; 1999 Jun 16; 13(4):301-10. PubMed ID: 10220144
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