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Rigshospitalet - en del af Københavns Universitetshospital
Udgivet

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

DOI

  1. Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  2. Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  3. Dominant optic atrophy in Denmark - report of 15 novel mutations in OPA1, using a strategy with a detection rate of 90%

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  4. Identification of 3 novel VHL germ-line mutations in Danish VHL patients

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Vis graf over relationer
Atrial fibrillation (AF) is the most common arrhythmia. The potassium current IKs is essential for cardiac repolarization. Gain-of-function mutations in KV7.1, the pore-forming α-subunit of the IKs channel, have been associated with AF. We hypothesized that early-onset lone AF is associated with mutations in the IKs channel regulatory subunit KCNE1.
OriginalsprogEngelsk
TidsskriftB M C Medical Genetics
Vol/bind13
Sider (fra-til)24
ISSN1471-2350
DOI
StatusUdgivet - 2012

ID: 36810723