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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Detalles Bibliográficos
Autores principales: Amirian, Azam, Zafari, Zahra, Karimipoor, Morteza, Kordafshari, Alireza, Dalili, Mohammad, Saber, Siamak, Fazelifar, Amir Farjam, Zeinali, Sirous
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pasteur Institute 2019
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462296/
https://www.ncbi.nlm.nih.gov/pubmed/30797226
http://dx.doi.org/10.29252/.23.3.228

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462296/
https://www.ncbi.nlm.nih.gov/pubmed/30797226
http://dx.doi.org/10.29252/.23.3.228

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