(Q33174117)

23 July 2017

title

Locus heterogeneity of autosomal dominant long QT syndrome (English)

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23 July 2017

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M Curran

1

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23 July 2017

D Atkinson

2

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23 July 2017

K Timothy

3

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23 July 2017

G M Vincent

4

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23 July 2017

A J Moss

5

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23 July 2017

M Leppert

6

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23 July 2017

M Keating

7

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23 July 2017

language of work or name

English

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publication date

1 August 1993

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Journal of Clinical Investigation

23 July 2017

published in

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23 July 2017

volume

92

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23 July 2017

issue

2

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23 July 2017

page(s)

799-803

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A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN

23 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=294917

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval 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=294917

Isolation and preliminary characterization of a human transforming gene from T24 bladder carcinoma cells

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=294917

Unilateral Cervicothoracic Sympathetic Ganglionectomy for the Treatment of Long QT Interval Syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=294917

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=294917

The idiopathic long QT syndrome: pathogenetic mechanisms and therapy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=294917

Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=294917

Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene (TH).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=294917

Dinucleotide repeat polymorphism at the D11S860 locus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=294917

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=294917

CONGENITAL CARDIAC ARRHYTHMIA

21 June 2018

1 reference

12 December 2020

Functional distribution of right and left stellate innervation to the ventricles. Production of neurogenic electrocardiographic changes by unilateral alteration of sympathetic tone

1 reference

12 December 2020

Assignment of the polymorphic intestinal mucin gene (MUC2) to chromosome 11p15

1 reference

12 December 2020

Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

1 reference

12 December 2020

Effects of exercise on heart rate, QT, QTc and QT/QS2 in the Romano-Ward inherited long QT syndrome

1 reference

12 December 2020

Long QT and Harvey-ras

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12 December 2020

Identifiers

DOI

10.1172/JCI116653

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23 July 2017

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23 July 2017

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