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Different clinicopathological features between Japanese siblings with facioscapulohumeral muscular dystrophy 2 with a novel nonsense SMCHD1 mutation (Arg552∗)
Ohta, Yasuyuki, Tadokoro, Koh, Sasaki, Ryo, Takahashi, Yoshiaki, Sato, Kota, Takemoto, Mami, Hishikawa, Nozomi, Shang, Jingwei, Yamashita, Toru, Takehisa, Yasushi, Nishino, Ichizo, Abe, KojiLanguage:
english
Journal:
Journal of Clinical Neuroscience
DOI:
10.1016/j.jocn.2018.10.021
Date:
October, 2018
File:
PDF, 987 KB
english, 2018