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

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 (4). 553 - 561 (9). ISSN 1547-5271 https://doi.org/10.1016/j.hrthm.2008.01.020
SGUL Authors: Homfray, Tessa

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Item Type: Article
Additional Information: PubMed ID: 18362022
Keywords: Abortion, Spontaneous, Adult, Codon, Nonsense, Consanguinity, Death, Sudden, Cardiac, Ether-A-Go-Go Potassium Channels, Female, Fetal Death, Glutamine, Homozygote, Humans, Infant, Newborn, Long QT Syndrome, Male, Pedigree, Pilot Projects, Polymorphism, Genetic, Pregnancy, Pregnancy Trimester, Third, Recurrence, Risk Factors, Science & Technology, Life Sciences & Biomedicine, Cardiac & Cardiovascular Systems, Cardiovascular System & Cardiology, long QT syndrome, sudden cardiac death, electrophysiotogy, HERG, nonsense-mediated decay, LONG-QT SYNDROME, MESSENGER-RNA DECAY, I-KR, CHANNEL DYSFUNCTION, CARDIAC-ARRHYTHMIA, TRAFFICKING, BRADYCARDIA, KNOCKOUT, GENETICS, DISEASE, long QT syndrome, sudden cardiac death, electrophysiotogy, HERG, nonsense-mediated decay
Journal or Publication Title: HEART RHYTHM
ISSN: 1547-5271
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Dates:
DateEvent
1 April 2008Published
Web of Science ID: WOS:000254596600010
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URI: https://openaccess.sgul.ac.uk/id/eprint/440
Publisher's version: https://doi.org/10.1016/j.hrthm.2008.01.020

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