Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy-Reference-Cited by-同舟云学术

Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy

Published:2017-10-10 Issue:12 Volume:25 Page:1313-1323
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Robyns Tomas,Kuiperi Cuno,Breckpot Jeroen,Devriendt Koenraad^ORCID,Souche Erika,Van Cleemput Johan,Willems Rik,Nuyens Dieter,Matthijs Gert,Corveleyn Anniek

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/s41431-017-0004-3.pdf

Reference37 articles.

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3. Kapplinger JD, Tester DJ, Salisbury BA, et al. Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test. Heart Rhythm. 2009;6:1297–1303.

4. Richard P, Charron P, Carrier L, et al. Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation. 2003;107:2227–2232.

5. Koopmann TT, Alders M, Jongbloed RJ, et al. Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies. Heart Rhythm. 2006;3:52–55.

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