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Non-coding CGG repeat expansion in LOC642361/NUTM2B-AS1 is associated with a phenotype of oculopharyngodistal myopathy.

Xinyu GuJiaxi YuKexin JiaoJianwen DengXingyu XiaKai QiaoDongyue YueMingshi GaoChongbo ZhaoJihong DongGongchun HuangJingli ShanChuanzhu YanLi DiYuwei DaWenhua ZhuJianying XiZhaoxia Wang
Published in: Journal of medical genetics (2023)
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Keyphrases
  • late onset
  • muscular dystrophy
  • early onset
  • myasthenia gravis
  • duchenne muscular dystrophy