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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Veröffentlicht in:Iran Biomed J
Hauptverfasser: Amirian, Azam, Zafari, Zahra, Karimipoor, Morteza, Kordafshari, Alireza, Dalili, Mohammad, Saber, Siamak, Fazelifar, Amir Farjam, Zeinali, Sirous
Format: Artigo
Sprache:Inglês
Veröffentlicht: Pasteur Institute 2019
Schlagworte:
Short Communication
Online Zugang: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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