(Q44757963)

6 December 2017

Cardiac ion channel gene mutations in Greek long QT syndrome patients (English)

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6 December 2017

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C-M Kotta

1

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6 December 2017

A Anastasakis

2

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6 December 2017

K Gatzoulis

3

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6 December 2017

J Papagiannis

4

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6 December 2017

P Geleris

5

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6 December 2017

C Stefanadis

6

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6 December 2017

1 January 2010

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Journal of Applied Genetics

6 December 2017

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6 December 2017

51

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6 December 2017

4

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6 December 2017

515-518

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https://scigraph.springernature.com/pub.10.1007/bf03208882

6 December 2017

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cites work

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

1 reference

https://api.crossref.org/works/10.1007%2FBF03208882

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03208882

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/10.1007%2FBF03208882

Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03208882

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03208882

Cost-effectiveness analysis of genetic testing for familial long QT syndrome in symptomatic index cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03208882

Role of genetic analyses in cardiology: part I: mendelian diseases: cardiac channelopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03208882

Risk stratification in the long-QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03208882

Diagnostic criteria for the long QT syndrome. An update

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03208882

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03208882

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03208882

Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing

21 January 2018

1 reference

12 December 2020

Low penetrance in the long-QT syndrome: clinical impact

1 reference

12 December 2020

Defective human Ether-à-go-go-related gene trafficking linked to an endoplasmic reticulum retention signal in the C terminus

1 reference

12 December 2020

Phenotype reveals genotype in a Greek long QT syndrome family

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03208882

1 reference

6 December 2017

1 reference