Records 1 - 4 (of 4 Records)
|Query Trace: Channelopathies and MYH7[original query]|
| A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular Noncompaction.
Journal of the American Heart Association 2017 Aug 6 (9): .
Wang Ce, Hata Yukiko, Hirono Keiichi, Takasaki Asami, Ozawa Sayaka Watanabe, Nakaoka Hideyuki, Saito Kazuyoshi, Miyao Nariaki, Okabe Mako, Ibuki Keijiro, Nishida Naoki, Origasa Hideki, Yu Xianyi, Bowles Neil E, Ichida Fukiko,
| Identification of pathogenic variants in genes related to channelopathy and cardiomyopathy in Korean sudden cardiac arrest survivors.
Journal of human genetics 2017 Jun 62 (6): 615-620.
Song Ju Sun, Kang Jong-Sun, Kim Young-Eun, Park Seung-Jung, Park Kyoung-Min, Huh June, Kim June Soo, Cho Hana, Ki Chang-Seok, On Young Ke
| Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience.
Hong Kong medical journal = Xianggang yi xue za zhi 2018 3 24 (4): 340-349.
Mak C M, Chen S Pl, Mok N S, Siu W K, Lee H Hc, Ching C K, Tsui P T, Fong N C, Yuen Y P, Poon W T, Law C Y, Chong Y K, Chan Y W, Yung T C, Fan K Yy, Lam C
| Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel.
Orphanet journal of rare diseases 2022 10 17 (1): 394.
Chen Jia, Li Hong, Guo Sicheng, Yang Zhe, Sun Shaoping, Zeng JunJie, Gou Hongjuan, Chen Yechang, Wang Feng, Lin Yanping, Huang Kun, Yue Hong, Ma Yuting, Lin Yu