Characterization and haplotype study of 6 novel STR markers related to the KCNQ1 gene in heterogeneous cardiovascular disorders in the Iranian population

The KCNQ1 gene has a significant role in long QT syndrome, Jervell and Lange-Nielsen syndrome, familial atrial fibrillation, and short QT syndrome. Analyzing such heterogeneous disorders, six novel short tandem repeat (STR) markers around the KCNQ1 gene were found and evaluated in a healthy populati...

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Detalles Bibliográficos
Autores principales: AMIRIAN, Azam, ZAFARI, Zahra, SHARIFI, Zohreh, KORDAFSHARI, Alireza, KARIMIPOOR, Morteza, ZEINALI, Sirous
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018329/
https://www.ncbi.nlm.nih.gov/pubmed/30866607
http://dx.doi.org/10.3906/sag-1805-43

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018329/
https://www.ncbi.nlm.nih.gov/pubmed/30866607
http://dx.doi.org/10.3906/sag-1805-43

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