Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families

BACKGROUND: Long QT syndrome (LQTS) is characterized by the prolongation of QT interval, which results in syncope and sudden cardiac death in young people. KCNQ1 is the most common gene responsible for this syndrome. METHODS: Molecular investigation was performed by DNA Sanger sequencing in Iranian...

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Detalhes bibliográficos
Publicado no:Iran Biomed J
Main Authors: Amirian, Azam, Zafari, Zahra, Karimipoor, Morteza, Kordafshari, Alireza, Dalili, Mohammad, Saber, Siamak, Fazelifar, Amir Farjam, Zeinali, Sirous
Formato: Artigo
Idioma:Inglês
Publicado em: Pasteur Institute 2019
Assuntos:
Short Communication
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6462296/
https://ncbi.nlm.nih.gov/pubmed/30797226
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.29252/.23.3.228
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