Genetic testing for long QT syndrome and the category of cardiac ion channelopathies

Cardiac ion channel mutational analysis is a category of genetic testing used in clinical practice for determining the status of long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia, and Brugada syndrome genes in blood, saliva, or tissue from patients and family...

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Detalles Bibliográficos
Autores principales: Modell, Stephen M., Bradley, David J., Lehmann, Michael H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Diagnostic
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392134/
https://www.ncbi.nlm.nih.gov/pubmed/22872816
http://dx.doi.org/10.1371/4f9995f69e6c7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392134/
https://www.ncbi.nlm.nih.gov/pubmed/22872816
http://dx.doi.org/10.1371/4f9995f69e6c7

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