Cargando…
Chromosome 4q25 Variant rs6817105 Bring Sinus Node Dysfunction and Left Atrial Enlargement
Genome-wide association studies have reported a strong association of the single nucleotide polymorphism (SNP) rs6817105 (T > C) on chromosome 4q25 with atrial fibrillation (AF), but phenotype alterations conferred by this SNP have not been described. We genotyped SNP rs6817105 and examined the r...
Autores principales: | Tomomori, Shunsuke, Nakano, Yukiko, Ochi, Hidenori, Onohara, Yuko, Sairaku, Akinori, Tokuyama, Takehito, Motoda, Chikaaki, Matsumura, Hiroya, Amioka, Michitaka, Hironobe, Naoya, Okubo, Yousaku, Okamura, Shou, Kawazoe, Hiroshi, Nishiyama, Yukie, Tahara, Hidetoshi, Chayama, Kazuaki, Kihara, Yasuki |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167315/ https://www.ncbi.nlm.nih.gov/pubmed/30275471 http://dx.doi.org/10.1038/s41598-018-32453-8 |
Ejemplares similares
-
Ser96Ala genetic variant of the human histidine-rich calcium-binding protein is a genetic predictor of recurrence after catheter ablation in patients with paroxysmal atrial fibrillation
por: Amioka, Michitaka, et al.
Publicado: (2019) -
Maintenance of low inflammation level by the ZFHX3 SNP rs2106261 minor allele contributes to reduced atrial fibrillation recurrence after pulmonary vein isolation
por: Tomomori, Shunsuke, et al.
Publicado: (2018) -
H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promoters
por: Matsumura, Hiroya, et al.
Publicado: (2017) -
Genetic variations of aldehyde dehydrogenase 2 and alcohol dehydrogenase 1B are associated with the etiology of atrial fibrillation in Japanese
por: Nakano, Yukiko, et al.
Publicado: (2016) -
Plasma MicroRNAs as noninvasive diagnostic biomarkers in patients with Brugada syndrome
por: Ikeuchi, Yoshihiro, et al.
Publicado: (2022)