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
Full text not available from this repository.
| Item Type: |
Article
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| 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 |
| Related URLs: |
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| Dates: |
| Date | Event |
|---|
| 1 April 2008 | Published |
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| 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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