在前两个印度家庭中与TMEM151A相关的松性运动障碍
Revathi Sampath1, Prabhakara Somanna1, Anbazhagan Kolandaswamy2
1Department of Biotechnology, Dr.M.G.R. Educational and Research Institute, Chennai, India; Department of Genetics, RajaRajeswari Medical College and Hospital, Bangalore, India.
在TMEM151A的遗传变异与 Paroxysmal Kinesigenic Dyskinesia有关. 这项研究在一个家族中发现了已知的TMEM151A变异,在另一个家族中发现了新的变异,从而进一步了解了这种神经疾病.
科学领域:
- 遗传学
- 神经学
- 分子生物学
背景情况:
- 帕洛克斯基因性运动障碍 (PKD) 是一种罕见的神经运动障碍.
- 虽然PRRT2变异已被确定为PKD的原因,但其他遗传因素仍在研究中.
- TMEM151A已与PKD的发病有关.
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