Different clinicopathological features between Japanese siblings with facioscapulohumeral muscular dystrophy 2 with a novel nonsense SMCHD1 mutation (Arg552*)

导出原文传递

翻译打印收藏纠错

作者： Ohta, Yasuyuki ^[1] ; Tadokoro, Koh ^[2] ; Sasaki, Ryo ^[3] ; Takahashi, Yoshiaki ; Sato, Kota ; Takemoto, Mami ; Hishikawa, Nozomi ; Shang, Jingwei ; Yamashita, Toru ; Takehisa, Yasushi ; Nishino, Ichizo ; Abe, Koji

作者单位： Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Dept Neuromuscular Res, Tokyo, Japan ^[1] Japanese Red Cross Okayama Hosp, Dept Neurol, Okayama, Japan ^[2] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Neurol, 2-5-1 Shikata Cho, Okayama 7008558 ^[3]

关键词 D4Z4 DNA methylation FSHD2 SMCHD1

发布时间 2019-05-22

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交

浏览1

Journal of clinical neuroscience

2018年58卷

215-217页

相似文献

中文期刊
外文期刊
学位论文
会议论文

检索历史清除

Different clinicopathological features between Japanese siblings with facioscapulohumeral muscular dystrophy 2 with a novel nonsense SMCHD1 mutation (Arg552*)

Journal of clinical neuroscience

相似文献

Journal of clinical neuroscience

相关期刊

参考文献：
指定格式：	NoteExpress EndNote RefWorks NoteFirst

检索历史 清除

Different clinicopathological features between Japanese siblings with facioscapulohumeral muscular dystrophy 2 with a novel nonsense SMCHD1 mutation (Arg552*)

Journal of clinical neuroscience

相似文献

Journal of clinical neuroscience

相关期刊

检索历史清除