(Q48045058)

7 February 2018

title

Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias. (English)

1 reference

7 February 2018

1 reference

6

1 reference

7 February 2018

author name string

Wollnik B

1

1 reference

7 February 2018

Schroeder BC

2

1 reference

7 February 2018

Kubisch C

3

1 reference

7 February 2018

Esperer HD

4

1 reference

7 February 2018

Wieacker P

5

1 reference

7 February 2018

publication date

1 October 1997

1 reference

7 February 2018

number of pages

7

1 reference

based on heuristic

inferred from page(s)

published in

Human Molecular Genetics

1 reference

7 February 2018

volume

6

1 reference

7 February 2018

page(s)

1943-1949

1 reference

7 February 2018

issue

11

1 reference

7 February 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

Molecular mechanism for an inherited cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

HERG, a human inward rectifier in the voltage-gated potassium channel family

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

Cloning of a membrane protein that induces a slow voltage-gated potassium current

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

A family of potassium channel genes related to eag in Drosophila and mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

Mutations in the K+ channel signature sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

Interactions of the H5 pore region and hydroxylamine with N-type inactivation in the Shaker K+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

Diagnostic criteria for the long QT syndrome. An update

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

Heteromultimeric CLC chloride channels with novel properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1943

21 January 2018

Identifiers

DOI

10.1093/HMG/6.11.1943

1 reference

7 February 2018

release_xfmnsyfgkfdghlbh6kjrhwgfiy

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/xfmnsyfgkfdghlbh6kjrhwgfiy

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

9302275

1 reference

7 February 2018