在GOSR2相关的渐进性肌性中,新的遗传和表型扩张
Lea Hentrich1,2,3, Mered Parnes4, Timothy Edward Lotze4
1Department of Pediatrics, Faculty of Medicine and University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.
戈尔吉SNAP受体复合体成员2基因 (GOSR2) 的新遗传变异扩大了对GOSR2相关疾病的理解,包括,发育迟缓和运动障碍.
科学领域:
- 遗传学 遗传学 是一个
- 神经学 神经学
- 分子生物学分子生物学
背景情况:
- 随着神经退行症的渐进性肌性与GOSR2基因中的双变异有关.
- 临床特征通常包括早期发作的,反,发作,脊椎病,筋障碍症和肌.
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