Pharmacogenetics of cardiac K(+) channels (Q33145998)

22 July 2017

title

Pharmacogenetics of cardiac K(+) channels (English)

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22 July 2017

Escande D

1

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22 July 2017

publication date

1 December 2000

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European Journal of Pharmacology

22 July 2017

language of work or name

English

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published in

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22 July 2017

volume

410

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22 July 2017

issue

2-3

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22 July 2017

page(s)

281-287

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publication type of scholarly work

22 July 2017

review article

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

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

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Proarrhythmia With Class III Antiarrhythmic Drugs: Types, Risks, and Management

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

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Age-gender influence on the rate-corrected QT interval and the QT-heart rate relation in families with genotypically characterized long QT syndrome

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Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias

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

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

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7 January 2021

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10.1016/S0014-2999(00)00821-9

7 January 2021

Identifiers

DOI

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22 July 2017

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