(Q48944651)

17 February 2018

title

A de novo missense mutation of human cardiac Na+ channel exhibiting novel molecular mechanisms of long QT syndrome. (English)

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17 February 2018

author name string

Makita N

1

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17 February 2018

Shirai N

2

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17 February 2018

Nagashima M

3

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17 February 2018

Matsuoka R

4

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17 February 2018

Yamada Y

5

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17 February 2018

Tohse N

6

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17 February 2018

Kitabatake A

7

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17 February 2018

language of work or name

English

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publication date

1 February 1998

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17 February 2018

published in

FEBS Letters

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17 February 2018

volume

423

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17 February 2018

issue

1

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17 February 2018

page(s)

5-9

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17 February 2018

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

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

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

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Voltage clamping of Xenopus laevis oocytes utilizing agarose-cushion electrodes.

21 January 2018

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21 January 2018

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Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Multiple domains contribute to the distinct inactivation properties of human heart and skeletal muscle Na+ channels

21 January 2018

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Molecular determinants of beta 1 subunit-induced gating modulation in voltage-dependent Na+ channels.

7 January 2021

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Structure and function of voltage-dependent sodium channels: comparison of brain II and cardiac isoforms

7 January 2021

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10.1016/S0014-5793(98)00033-7

7 January 2021

Identifiers

DOI

1 reference

17 February 2018

PubMed ID

9506831

1 reference

17 February 2018