reference/2384706

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publicationName	Heart Rhythm
startingPage	212
bibliographicCitation	Crotti L, Lewandowska MA, Schwartz PJ, Insolia R, Pedrazzini M, Bussani E, Dagradi F, George AL, Pagani F. A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome. Heart Rhythm. 2009 Feb;6(2):212–8. doi: 10.1016/j.hrthm.2008.10.044. PMID: 19187913.
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date	200902
identifier	https://doi.org/10.1016/j.hrthm.2008.10.044 https://pubmed.ncbi.nlm.nih.gov/19187913
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language	English
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title	A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome
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