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

Joep Geraedts

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author name string

Roselie Jongbloed

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10 February 2018

Carlo Marcelis

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10 February 2018

Crool Velter

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10 February 2018

Pieter Doevendans

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10 February 2018

Joep Geraedts

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10 February 2018

Hubert Smeets

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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

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10 February 2018

issue

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10 February 2018

page(s)

382-391

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10 February 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Ion channels--basic science and clinical disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Novel KCNQ1 and HERG missense mutations in Dutch long-QT families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

A K+ channel splice variant common in human heart lacks a C-terminal domain required for expression of rapidly activating delayed rectifier current

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Cardiac conduction defects associate with mutations in SCN5A

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

KCNE1 mutations cause Jervell and Lange-Nielsen syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Diagnostic criteria for the long QT syndrome. An update

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Molecular basis of the long-QT syndrome associated with deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

A sodium-channel mutation causes isolated cardiac conduction disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

A pre-Columbian Y chromosome-specific transition and its implications for human evolutionary history

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Denaturing high-performance liquid chromatography: A review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Blind Analysis of Denaturing High-Performance Liquid Chromatography as a Tool for Mutation Detection

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Complete and rapid scanning of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by denaturing high-performance liquid chromatography (D-HPLC): major implications for genetic counselling

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Low penetrance in the long-QT syndrome: clinical impact

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

CONGENITAL CARDIAC ARRHYTHMIA

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

High and low annealing temperatures increase both specificity and yield in touchdown and stepdown PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10131

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7 January 2021

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Identifiers

DOI

10.1002/HUMU.10131

1 reference

10 February 2018

1 reference

10 February 2018