reference/29511457

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/29511457

Outgoing Links

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endingPage	2375
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issueIdentifier	21
pageRange	2366-2375
publicationName	Circulation
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bibliographicCitation	Crotti L, Spazzolini C, Schwartz PJ, Shimizu W, Denjoy I, Schulze-Bahr E, Zaklyazminskaya EV, Swan H, Ackerman MJ, Moss AJ, Wilde AA, Horie M, Brink PA, Insolia R, De Ferrari GM, Crimi G. The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification. Circulation. 2007 Nov 20;116(21):2366–75. doi: 10.1161/circulationaha.107.726950. PMID: 17984373.
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date	2007-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/17984373 https://doi.org/10.1161/circulationaha.107.726950
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification
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Total number of triples: 61.