Clinical and Genetic Analysis of Long QT Syndrome in Children from Six Families in Saudi Arabia: Are They Different?-Reference-Cited by-同舟云学术

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Clinical and Genetic Analysis of Long QT Syndrome in Children from Six Families in Saudi Arabia: Are They Different?

Published:2009-01-30 Issue:4 Volume:30 Page:490-501
ISSN:0172-0643
Container-title:Pediatric Cardiology
language:en
Short-container-title:Pediatr Cardiol

Author:

Bhuiyan Zahurul A.,Al-Shahrani Safar,Al-Khadra Ayman S.,Al-Ghamdi Saleh,Al-Khalaf Khalaf,Mannens Marcel M. A. M.,Wilde Arthur A. M.,Momenah Tarek S.

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00246-008-9377-y.pdf

Reference49 articles.

1. Al-Gazali L, Hamamy H, Al-Arrayad S (2006) Genetic disorders in the Arab world. BMJ 333:831–834

2. Bazett H (1920) An analysis of the time relationships of electrocardiograms. Heart 7:353–370

3. Bhuiyan ZA, Momenah TS, Gong Q, Amin AS, Ghamdi SA, Carvalho JS, Homfray T, Mannens MM, Zhou Z, Wilde AA (2008) Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation. Heart Rhythm 5:553–561

4. Bhuiyan ZA, Momenah TS, Amin AS, Al-Khadra AS, Alders M, Wilde AA, Mannens MM (2008) An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome. Prog Biophys Mol Biol [Epub ahead of print]

5. Chen Q, Zhang D, Gingell RL, Moss AJ, Napolitano C, Priori SG, Schwartz PJ, Kehoe E, Robinson JL, Schulze-Bahr E, Wang Q, Towbin JA (1999) Homozygous deletion in KVLQT1 associated with Jervell and Lange–Nielsen syndrome. Circulation 99:1344–1347

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Long-QT founder variant T309I-Kv7.1 with dominant negative pattern may predispose delayed afterdepolarizations under β-adrenergic stimulation;Scientific Reports;2021-02-11

2. Molecular autopsy: using the discovery of a novel de novo pathogenic variant in the KCNH2 gene to inform healthcare of surviving family;Heliyon;2018-12

3. Clinical profile and mutation spectrum of long QT syndrome in Saudi Arabia: The impact of consanguinity;Heart Rhythm;2017-08

4. Molecular insight into heart development and congenital heart disease: An update review from the Arab countries;Trends in Cardiovascular Medicine;2015-05

5. Genotype-phenotype analysis of Jervell and Lange-Nielsen syndrome in six families from Saudi Arabia;Clinical Genetics;2013-12-27

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