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Mutation detection in long QT syndrome: a comprehensive set of primers and PCR conditions

Syrris, P; Murray, A; Carter, ND; McKenna, WM; Jeffery, S; (2001) Mutation detection in long QT syndrome: a comprehensive set of primers and PCR conditions. J MED GENET , 38 (10) 705 - 710.

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Type: Article
Title: Mutation detection in long QT syndrome: a comprehensive set of primers and PCR conditions
Keywords: LANGE-NIELSEN-SYNDROME, POTASSIUM CHANNEL GENE, GENOMIC ORGANIZATION, CARDIAC-ARRHYTHMIA, SCN5A MUTATIONS, MOLECULAR-BASIS, SODIUM-CHANNEL, CAUSE JERVELL, NA+ CHANNEL, ROMANO-WARD
UCL classification: UCL > School of Life and Medical Sciences
UCL > School of Life and Medical Sciences > Faculty of Population Health Sciences
UCL > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Cardiovascular Science
URI: http://discovery.ucl.ac.uk/id/eprint/82064
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