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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Iran Biomed J
Prif Awduron: Amirian, Azam, Zafari, Zahra, Karimipoor, Morteza, Kordafshari, Alireza, Dalili, Mohammad, Saber, Siamak, Fazelifar, Amir Farjam, Zeinali, Sirous
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Pasteur Institute 2019
Pynciau:
Short Communication
Mynediad Ar-lein: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
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg