(Q48276367)

10 February 2018

title

DHPLC analysis of potassium ion channel genes in congenital long QT syndrome. (English)

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10 February 2018

5

Joep Geraedts

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author name string

Roselie Jongbloed

1

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10 February 2018

Carlo Marcelis

2

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10 February 2018

Crool Velter

3

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10 February 2018

Pieter Doevendans

4

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10 February 2018

Joep Geraedts

5

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10 February 2018

Hubert Smeets

6

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10 February 2018

publication date

1 November 2002

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10 February 2018

published in

Human Mutation

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10 February 2018

volume

20

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10 February 2018

page(s)

382-391

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10 February 2018

issue

5

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10 February 2018

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

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Mutation analysis of the hamartin gene using denaturing high performance liquid chromatography

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Evaluation of DHPLC analysis in mutational scanning of Notch3, a gene with a high G-C content

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Hypokalemia-induced long QT syndrome with an underlying novel missense mutation in S4-S5 linker of KCNQ1

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/HUMU.10131

1 reference

10 February 2018

PubMed ID

12402336

1 reference

10 February 2018