reference/23697597

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/23697597

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publicationName	Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc
startingPage	e12694
bibliographicCitation	Lin Y, Zhao T, He S, Huang J, Liu Q, Yang Z, Qin J, Yu N, Lu H, Lin X. Compound and heterozygous mutations of KCNQ1 in long QT syndrome with familial history of unexplained sudden death: Identified by analysis of whole exome sequencing and predisposing genes. Ann Noninvasive Electrocardiol. 2020 Jan;25(1):e12694. PMID: 31565860; PMCID: PMC7358849.
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date	2019-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC7358849 https://doi.org/10.1111/anec.12694 https://pubmed.ncbi.nlm.nih.gov/31565860
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Compound and heterozygous mutations of KCNQ1 in long QT syndrome with familial history of unexplained sudden death: Identified by analysis of whole exome sequencing and predisposing genes
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Total number of triples: 49.