Found: 7
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Prevalence, mutation spectrum, and cardiac phenotype of the Jervell and Lange-Nielsen syndrome in Sweden.
- Published in:
- EP: Europace, 2012, v. 14, n. 12, p. 1799, doi. 10.1093/europace/eus111
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- Publication type:
- Article
Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families.
- Published in:
- BMC Cardiovascular Disorders, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2261-14-22
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- Publication type:
- Article
Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families.
- Published in:
- 2014
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- Publication type:
- journal article
Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing.
- Published in:
- BMC Cardiovascular Disorders, 2012, v. 12, n. 1, p. 95, doi. 10.1186/1471-2261-12-95
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- Publication type:
- Article
Vectorcardiographic Recordings of the Q-T Interval in a Pediatric Long Q-T Syndrome Population.
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- Pediatric Cardiology, 2013, v. 34, n. 2, p. 245, doi. 10.1007/s00246-012-0425-2
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- Publication type:
- Article
To Modify or Not to Modify: Allele-Specific Effects of 3'UTR- Single Nucleotide Polymorphisms on Clinical Phenotype in a Long QT 1 Founder Population Segregating a Dominant-Negative Mutation.
- Published in:
- 2022
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- Publication type:
- journal article
QT correction using Bazett's formula remains preferable in long QT syndrome type 1 and 2.
- Published in:
- Annals of Noninvasive Electrocardiology, 2021, v. 26, n. 1, p. 1, doi. 10.1111/anec.12804
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- Publication type:
- Article