(Q33148338)

22 July 2017

title

KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population (English)

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22 July 2017

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Wenling Liu

1

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22 July 2017

Junguo Yang

2

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22 July 2017

Dayi Hu

3

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22 July 2017

Cailian Kang

4

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22 July 2017

Cuilan Li

5

1 reference

22 July 2017

Shuoyan Zhang

6

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22 July 2017

Ping Li

7

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22 July 2017

Zhijian Chen

8

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22 July 2017

Xuguang Qin

9

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22 July 2017

Kang Ying

10

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22 July 2017

Yuntian Li

11

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22 July 2017

Yushu Li

12

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22 July 2017

Zhiming Li

13

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22 July 2017

Xin Cheng

14

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22 July 2017

Lei Li

15

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22 July 2017

Yu Qi

16

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22 July 2017

Shenghan Chen

17

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22 July 2017

Qing Wang

18

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22 July 2017

publication date

1 December 2002

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22 July 2017

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22 July 2017

volume

20

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22 July 2017

issue

6

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22 July 2017

page(s)

475-476

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

22 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1679868

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1679868

Inherited long QT syndromes: a paradigm for understanding arrhythmogenesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1679868

Mechanisms and management of proarrhythmia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1679868

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1679868

The molecular genetics of the long QT syndrome: genes causing fainting and sudden death

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1679868

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1679868

Diagnostic criteria for the long QT syndrome. An update

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1679868

The long QT syndrome. Prospective longitudinal study of 328 families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1679868

21 June 2018

The long Q-T syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1679868

Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12442276

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/HUMU.9085

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22 July 2017

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22 July 2017

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