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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Detalhes bibliográficos
Publicado no: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
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2018
Assuntos:
Research Article
Acesso em linha: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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