与MCM3AP变种相关的两个周期性病例
Tatsuya Oishi1, Jennifer Pagano2, Cody Sellers3
1Department of Neurology, Mayo Clinic, Rochester MN.
Journal of clinical neuromuscular disease
|August 23, 2023
概括
MCM3AP基因中的遗传变异与周期性有关,这是一种罕见的神经肌肉疾病,会导致偶发性衰弱. 这项研究确定了两个患有周期性症状的患者的MCM3AP基因变异.
科学领域:
- 遗传学 是一个遗传学.
- 神经学 神经学
- 分子生物学分子生物学
背景情况:
- 周期性是一种罕见的遗传神经肌肉疾病.
- 软弱的发作往往是由环境因素和生理压力引发的.
- 虽然离子通道基因突变很常见,但其他遗传因素正在被调查.
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