(Q47398470)

English

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

scientific article published in January 2004

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scholarly article

1 reference

Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

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 (English)

1 reference

Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

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1 reference

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author name string

Heidi Fodstad

1

1 reference

Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

Heikki Swan

2

1 reference

Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

Päivi Laitinen

3

1 reference

Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

Kirsi Piippo

4

1 reference

Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

Kristian Paavonen

5

1 reference

Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

Matti Viitasalo

6

1 reference

Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

Lauri Toivonen

7

1 reference

Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

Kimmo Kontula

8

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Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

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publication date

1 January 2004

1 reference

Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

Annals of Medicine

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Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

36 Suppl 1

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Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

53-63

1 reference

Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

Idiopathic long QT syndrome: progress and questions

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

The long QT syndrome: ion channel diseases of the heart

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Mutations in the hminK gene cause long QT syndrome and suppress IKs function

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Effect of the antimalarial drug halofantrine in the long QT syndrome due to a mutation of the cardiac sodium channel gene SCN5A.

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518X.

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel.

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Natural history of Brugada syndrome: insights for risk stratification and management

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

A sodium-channel mutation causes isolated cardiac conduction disease

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Exclusion of KCNE1 (IsK) as a Candidate Gene for Jervell and Lange-Nielsen Syndrome

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Association between HERG K897T polymorphism and QT interval in middle-aged Finnish women

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Functional characterization of the common amino acid 897 polymorphism of the cardiac potassium channel KCNH2 (HERG).

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5A.

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032689

21 January 2018

Identifiers

10.1080/17431380410032689

1 reference

Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

1 reference

Europe PubMed Central

15 January 2018

http://europepmc.org/abstract/MED/15176425

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