Rydberg Annika
Biographic Data
| ID | 196521 |
|---|---|
| NAME | Rydberg Annika |
| GIVEN NAMES | Rydberg |
| FAMILY NAME | Annika |
| SIGNATURE | ANNIKA R |
| AFFILIATIONS | University of Auckland |
| VERIFIED | No |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 1 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2020 |
| LATEST PUBLICATION YEAR | 2020 |
| H-INDEX | 0 |
LQTS founder population in Northern Sweden - the natural history of a potentially fatal inherited cardiac disorder
Long QT Syndrome (LQTS) is an autosomal dominant inherited cardiac disorder associated with life-threatening arrhythmias. In northern Sweden, a LQTS founder mutation (p.Y111C, KCNQ1 gene) was verified by genetic haplotype analysis and genealogical studies, and a common ancestor couple was identified. Clinical studies of this population revealed an apparent mild phenotype. However, due to early commencement of prophylactic treatment, the natural h…
No prominent works on this page.
LQTS founder population in Northern Sweden - the natural history of a potentially fatal inherited cardiac disorder
Long QT Syndrome (LQTS) is an autosomal dominant inherited cardiac disorder associated with life-threatening arrhythmias. In northern Sweden, a LQTS founder mutation (p.Y111C, KCNQ1 gene) was verified by genetic haplotype analysis and genealogical studies, and a common ancestor couple was identified. Clinical studies of this population revealed an apparent mild phenotype. However, due to early commencement of prophylactic treatment, the natural h…
Biology (1 works) · Cardiac electrophysiology and arrhythmias (1 works) · Demography (1 works) · Family history (1 works) · Founder effect (1 works) · Gene (1 works) · Genetics (1 works) · Genotype (1 works) · Haplotype (1 works) · Internal Medicine (1 works)