(Q33148873)

22 July 2017

title

Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome (English)

1 reference

voltage-gated potassium channel

22 July 2017

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12710526

26 December 2023

1 reference

26 December 2023

1 reference

26 December 2023

4

Robert Hegele

0 references

author name string

Dominic Deschênes

1

1 reference

22 July 2017

Said Acharfi

2

1 reference

22 July 2017

Valerie Pouliot

3

1 reference

22 July 2017

Andrew Krahn

5

1 reference

22 July 2017

Pascal Daleau

6

1 reference

22 July 2017

Mohamed Chahine

7

1 reference

22 July 2017

Robert Hegele

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12710526

26 December 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12710526

26 December 2023

publication date

1 February 2003

1 reference

full work available at URL

22 July 2017

http://www.nrcresearchpress.com/doi/pdf/10.1139/y02-162

1 reference

Canadian Journal of Physiology and Pharmacology

26 December 2023

published in

1 reference

22 July 2017

volume

81

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22 July 2017

issue

2

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22 July 2017

page(s)

129-134

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

22 July 2017

cites work

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

A novel mutation in KVLQT1, L122P, found in a family with autosomal dominant long QT syndrome

21 January 2018

1 reference

Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block

21 January 2018

1 reference

A recessive variant of the Romano-Ward long-QT syndrome?

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Functional effects of mutations in KvLQT1 that cause long QT syndrome.

21 January 2018

1 reference

Clinical aspects of the idiopathic long QT syndrome

21 January 2018

1 reference

21 January 2018

1 reference

Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk

21 January 2018

1 reference

American Journal of Physiology

21 January 2018

5

279

H1748

Ficker E.

2000

1 reference

26 December 2023

Identifiers

DOI

10.1139/Y02-162

1 reference

release_r3iuklbdorasffa3rgkjy6ba2e

22 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/r3iuklbdorasffa3rgkjy6ba2e

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference