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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:Iran Biomed J
Main Authors: Amirian, Azam, Zafari, Zahra, Karimipoor, Morteza, Kordafshari, Alireza, Dalili, Mohammad, Saber, Siamak, Fazelifar, Amir Farjam, Zeinali, Sirous
Format: Artigo
Sprog:Inglês
Udgivet: Pasteur Institute 2019
Fag:
Short Communication
Online adgang: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
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker