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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado en:Iran Biomed J
Autores principales: Amirian, Azam, Zafari, Zahra, Karimipoor, Morteza, Kordafshari, Alireza, Dalili, Mohammad, Saber, Siamak, Fazelifar, Amir Farjam, Zeinali, Sirous
Formato: Artigo
Lenguaje:Inglês
Publicado: Pasteur Institute 2019
Materias:
Short Communication
Acceso en línea: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
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares