Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers (Q28292102)

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A Früh

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O-G Anfinsen

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K Gjesdal

5

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G Siem

6

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N Oyen

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G Greve

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A Carlsson

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T O Rognum

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M Hallerud

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E Kongsgård

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J P Amlie

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T P Leren

Scandinavian Journal of Clinical and Laboratory Investigation

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language of work or name

English

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publication date

2008

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published in

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volume

68

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issue

5

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page(s)

362-8

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cites work

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Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland

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Identifiers

DOI

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Consolidated OpenCitations Corpus – April 2017

3566387

3566387

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Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

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