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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1999 | 1 |
2000 | 1 |
2009 | 1 |
2011 | 1 |
2012 | 1 |
2024 | 0 |
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Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.
Hum Mutat. 1999;13(4):301-10. doi: 10.1002/(SICI)1098-1004(1999)13:4<301::AID-HUMU7>3.0.CO;2-V.
Hum Mutat. 1999.
PMID: 10220144
Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.
Splawski I, Shen J, Timothy KW, Lehmann MH, Priori S, Robinson JL, Moss AJ, Schwartz PJ, Towbin JA, Vincent GM, Keating MT.
Splawski I, et al.
Circulation. 2000 Sep 5;102(10):1178-85. doi: 10.1161/01.cir.102.10.1178.
Circulation. 2000.
PMID: 10973849
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Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.
Kapa S, Tester DJ, Salisbury BA, Harris-Kerr C, Pungliya MS, Alders M, Wilde AA, Ackerman MJ.
Kapa S, et al.
Circulation. 2009 Nov 3;120(18):1752-60. doi: 10.1161/CIRCULATIONAHA.109.863076. Epub 2009 Oct 19.
Circulation. 2009.
PMID: 19841300
Free PMC article.
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Use of mutant-specific ion channel characteristics for risk stratification of long QT syndrome patients.
Jons C, O-Uchi J, Moss AJ, Reumann M, Rice JJ, Goldenberg I, Zareba W, Wilde AA, Shimizu W, Kanters JK, McNitt S, Hofman N, Robinson JL, Lopes CM.
Jons C, et al.
Sci Transl Med. 2011 Mar 30;3(76):76ra28. doi: 10.1126/scitranslmed.3001551.
Sci Transl Med. 2011.
PMID: 21451124
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Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndrome.
Giudicessi JR, Kapplinger JD, Tester DJ, Alders M, Salisbury BA, Wilde AA, Ackerman MJ.
Giudicessi JR, et al.
Circ Cardiovasc Genet. 2012 Oct 1;5(5):519-28. doi: 10.1161/CIRCGENETICS.112.963785. Epub 2012 Sep 4.
Circ Cardiovasc Genet. 2012.
PMID: 22949429
Free PMC article.
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