Mechanistic basis for the pathogenesis of long QT syndrome associated with a common splicing mutation in KCNQ1 gene. (Q48801863)

15 February 2018

title

Mechanistic basis for the pathogenesis of long QT syndrome associated with a common splicing mutation in KCNQ1 gene. (English)

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2

Masaharu Akao

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author name string

Keiko Tsuji

1

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Takahiro M Ishii

3

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Seiko Ohno

4

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Takeru Makiyama

5

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Kotoe Takenaka

6

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Takahiro Doi

7

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Yoshisumi Haruna

8

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Hidetada Yoshida

9

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Toshihiro Nakashima

10

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Toru Kita

11

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Minoru Horie

12

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publication date

5 January 2007

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Journal of Molecular and Cellular Cardiology

published in

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volume

42

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issue

3

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page(s)

662-669

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CONGENITAL CARDIAC ARRHYTHMIA

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

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New mutations in the KVLQT1 potassium channel that cause long-QT syndrome

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Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome.

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7 January 2021

Identifiers

DOI

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15 February 2018

PubMed ID

17292394

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15 February 2018