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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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| Pubblicato in: | Iran Biomed J |
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| Autori principali: | , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Pasteur Institute
2019
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| Soggetti: | |
| Accesso online: | 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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