Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients: Koponen et al. Follow-up of adult LQTS patients

BACKGROUND: Long QT syndrome (LQTS) is an inherited cardiac disorder predisposing to sudden cardiac death (SCD). We studied factors affecting the clinical course of genetically confirmed patients, in particular those not receiving β-blocker treatment. In addition, an attempt was made to associate ri...

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Bibliografiske detaljer
Udgivet i:BMC Med Genet
Main Authors: Koponen, Mikael, Havulinna, Aki S., Marjamaa, Annukka, Tuiskula, Annukka M., Salomaa, Veikko, Laitinen-Forsblom, Päivi J., Piippo, Kirsi, Toivonen, Lauri, Kontula, Kimmo, Viitasalo, Matti, Swan, Heikki
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2018
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5887247/
https://ncbi.nlm.nih.gov/pubmed/29622001
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-018-0574-0
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