The KCNQ2 potassium channel: splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3 (Q28289632)

3

object named as

C Chouabe

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author name string

N Tinel

1

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I Lauritzen

2

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M Borsotto

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

5

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language of work or name

English

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publication date

6 November 1998

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published in

FEBS Letters

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volume

438

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issue

3

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page(s)

171-6

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cites work

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

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

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

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The structure, function and distribution of the mouse TWIK-1 K+ channel

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KvLQT1 potassium channel but not IsK is the molecular target for trans-6-cyano-4-(N-ethylsulfonyl-N-methylamino)-3-hydroxy-2,2-dimethyl- chromane

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Members of the RCK potassium channel family are differentially expressed in the rat nervous system.

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