Clinical and genetic analysis of long QT syndrome in children from six families in Saudi Arabia: are they different? (Q33157079)

22 July 2017

title

Clinical and genetic analysis of long QT syndrome in children from six families in Saudi Arabia: are they different? (English)

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22 July 2017

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7

Arthur A M Wilde

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22 July 2017

Zahurul A Bhuiyan

1

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22 July 2017

Safar Al-Shahrani

2

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22 July 2017

Ayman S Al-Khadra

3

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22 July 2017

Saleh Al-Ghamdi

4

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22 July 2017

Khalaf Al-Khalaf

5

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22 July 2017

Marcel M A M Mannens

6

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22 July 2017

Tarek S Momenah

8

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22 July 2017

publication date

30 January 2009

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22 July 2017

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22 July 2017

volume

30

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22 July 2017

issue

4

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22 July 2017

page(s)

490-501

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Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.

22 July 2017

cites work

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https://api.crossref.org/works/10.1007/S00246-008-9377-Y

Mutation of the Gene for I sK Associated With Both Jervell and Lange-Nielsen and Romano-Ward Forms of Long-QT Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00246-008-9377-Y

Homozygous premature truncation of the HERG protein : the human HERG knockout

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00246-008-9377-Y

A recessive variant of the Romano-Ward long-QT syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00246-008-9377-Y

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/10.1007/S00246-008-9377-Y

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/S00246-008-9377-Y

Mutation of an A-kinase-anchoring protein causes long-QT syndrome

21 January 2018

1 reference

12 December 2020

Regional specificity of human ether-a'-go-go-related gene channel activation and inactivation gating

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12 December 2020

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

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12 December 2020

KCNE1 mutations cause Jervell and Lange-Nielsen syndrome

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12 December 2020

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

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12 December 2020

Idiopathic long QT syndrome: asking the right question

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12 December 2020

Clinical practice. Long-QT syndrome

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12 December 2020

Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome

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12 December 2020

Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

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12 December 2020

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

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12 December 2020

Consanguinity among the Saudi Arabian population

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12 December 2020

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

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12 December 2020

The long QT syndrome with impaired atrioventricular conduction: a malignant variant in infants.

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12 December 2020

Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3

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12 December 2020

The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome

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12 December 2020

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

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12 December 2020

SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome

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12 December 2020

Long QT syndrome in children

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12 December 2020

Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome

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12 December 2020

The homozygous KCNQ1 gene mutation associated with recessive Romano-Ward syndrome

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12 December 2020

Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation

1 reference

12 December 2020

Selective knockout of mouse ERG1 B potassium channel eliminates I(Kr) in adult ventricular myocytes and elicits episodes of abrupt sinus bradycardia.

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12 December 2020

Compound mutations: a common cause of severe long-QT syndrome

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene

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12 December 2020

Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns

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12 December 2020

A newborn with a complex congenital heart disease, atrioventricular block, and torsade de pointes ventricular tachycardia

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12 December 2020

C-terminal HERG (LQT2) mutations disrupt IKr channel regulation through 14-3-3epsilon

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12 December 2020

A GRK5 polymorphism that inhibits beta-adrenergic receptor signaling is protective in heart failure

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12 December 2020

Nonsense mutations in hERG cause a decrease in mutant mRNA transcripts by nonsense-mediated mRNA decay in human long-QT syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome

1 reference

12 December 2020

Consanguinity and major genetic disorders in Saudi children: a community-based cross-sectional study.

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12 December 2020

Drugs that induce repolarization abnormalities cause bradycardia in zebrafish

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12 December 2020

Long QT syndrome and pregnancy

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12 December 2020

Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome

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12 December 2020

KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome

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12 December 2020

Genetic disorders in the Arab world

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12 December 2020

Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1).

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12 December 2020

10.1007/S00246-008-9377-Y

Identifiers

DOI

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Dimensions Publication ID

22 July 2017

1004303849

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