(Q59200879)

English

A KCNQ1 V205M missense mutation causes a high rate of long QT syndrome in a First Nations community of northern British Columbia: a community-based approach to understanding the impact

scientific article published on 01 July 2008

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scholarly article

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Europe PubMed Central

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9 January 2020

A KCNQ1 V205M missense mutation causes a high rate of long QT syndrome in a First Nations community of northern British Columbia: a community-based approach to understanding the impact (English)

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9 January 2020

long QT syndrome

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based on heuristic

inferred from title

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9 January 2020

Glen F. Tibbits

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9 January 2020

Shubhayan Sanatani

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9 January 2020

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Saman Rezazadeh

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9 January 2020

Jodene Eldstrom

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9 January 2020

Gwen Weget-Simms

4

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9 January 2020

Rosemarie Rupps

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9 January 2020

Zoe Dyer

6

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9 January 2020

Eric Accili

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9 January 2020

Brett Casey

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9 January 2020

Andrew Kmetic

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9 January 2020

David Fedida

12

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9 January 2020

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1 July 2008

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9 January 2020

Genetics in Medicine

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9 January 2020

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9 January 2020

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9 January 2020

545-550

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9 January 2020

https://scigraph.springernature.com/pub.10.1097/gim.0b013e31817c6b19

0 references

Molecular and cellular mechanisms of cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Cardiac channelopathies: it's in the genes

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

The long QT syndrome family of cardiac ion channelopathies: a HuGE review

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Compound mutations: a common cause of severe long-QT syndrome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Unraveling monogenic channelopathies and their implications for complex polygenic disease

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

The congenital long QT syndromes from genotype to phenotype: clinical implications

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Congenital and acquired long QT syndrome. Current concepts and management

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Assessment of QT interval and QT dispersion for prediction of all-cause and cardiovascular mortality in American Indians: The Strong Heart Study

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Molecular mechanism and functional significance of the MinK control of the KvLQT1 channel activity

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Dominant-negative KvLQT1 mutations underlie the LQT1 form of long QT syndrome.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

The N-terminal juxtamembranous domain of KCNQ1 is critical for channel surface expression: implications in the Romano-Ward LQT1 syndrome.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

A spectrum of functional effects for disease causing mutations in the Jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Functional effects of a KCNQ1 mutation associated with the long QT syndrome.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

DNA on loan: issues to consider when carrying out genetic research with aboriginal families and communities

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Participatory research maximises community and lay involvement. North American Primary Care Research Group

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Betaine, dimethyl sulfoxide, and 7-deaza-dGTP, a powerful mixture for amplification of GC-rich DNA sequences.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Restricting excessive cardiac action potential and QT prolongation: a vital role for IKs in human ventricular muscle.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Long QT syndrome. Why does sex matter?

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Female predominance and transmission distortion in the long-QT syndrome.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Clinical practice. Long-QT syndrome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Neural Control of Heart Rate Is an Arrhythmia Risk Modifier in Long QT Syndrome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Sudden infant death syndrome: how significant are the cardiac channelopathies?

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31817C6B19

21 January 2018

Community-based Participatory Research: Policy Recommendations for Promoting a Partnership Approach in Health Research

1 reference

28 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1080/13576280110051055

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