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Year | Number of Results |
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1995 | 1 |
2003 | 1 |
2004 | 1 |
2007 | 1 |
2024 | 0 |
PubMed (cited) for id: 600919
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Defining the cellular phenotype of "ankyrin-B syndrome" variants: human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes.
Circulation. 2007 Jan 30;115(4):432-41. doi: 10.1161/CIRCULATIONAHA.106.656512. Epub 2007 Jan 22.
Circulation. 2007.
PMID: 17242276
A cardiac arrhythmia syndrome caused by loss of ankyrin-B function.
Mohler PJ, Splawski I, Napolitano C, Bottelli G, Sharpe L, Timothy K, Priori SG, Keating MT, Bennett V.
Mohler PJ, et al.
Proc Natl Acad Sci U S A. 2004 Jun 15;101(24):9137-42. doi: 10.1073/pnas.0402546101. Epub 2004 Jun 3.
Proc Natl Acad Sci U S A. 2004.
PMID: 15178757
Free PMC article.
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Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death.
Mohler PJ, Schott JJ, Gramolini AO, Dilly KW, Guatimosim S, duBell WH, Song LS, Haurogné K, Kyndt F, Ali ME, Rogers TB, Lederer WJ, Escande D, Le Marec H, Bennett V.
Mohler PJ, et al.
Nature. 2003 Feb 6;421(6923):634-9. doi: 10.1038/nature01335.
Nature. 2003.
PMID: 12571597
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Mapping of a gene for long QT syndrome to chromosome 4q25-27.
Schott JJ, Charpentier F, Peltier S, Foley P, Drouin E, Bouhour JB, Donnelly P, Vergnaud G, Bachner L, Moisan JP, et al.
Schott JJ, et al.
Am J Hum Genet. 1995 Nov;57(5):1114-22.
Am J Hum Genet. 1995.
PMID: 7485162
Free PMC article.
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