Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia

BACKGROUND: One of the most common primary cardiac arrhythmia syndromes is autosomal dominant long QT syndrome, type 1 (LQT1), chiefly caused by mono‐allelic mutations in the KCNQ1 gene. Bi‐allelic mutations in the KCNQ1 gene are causal to Jervell and Lange‐Nielsen syndrome (JLNS), characterized by...

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Detalles Bibliográficos
Autores principales: Bdier, Amnah Y., Al‐Ghamdi, Saleh, Verma, Prashant K., Dagriri, Khalid, Alshehri, Bandar, Jiman, Omamah A., Ahmed, Sherif E., Wilde, Arthur A. M., Bhuiyan, Zahurul A., Al‐Aama, Jumana Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606890/
https://www.ncbi.nlm.nih.gov/pubmed/28944242
http://dx.doi.org/10.1002/mgg3.305

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606890/
https://www.ncbi.nlm.nih.gov/pubmed/28944242
http://dx.doi.org/10.1002/mgg3.305

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