斯克拉班-迪尔多夫智力障碍综合征相关的WDR26突变损害了CTLH E3复杂组件
Annette Gross1,2, Judith Müller2, Jakub Chrustowicz2
1Immunoregulation Research Group, Max Planck Institute of Biochemistry, Martinsried, Germany.
FEBS letters
|April 4, 2024
概括
在WDR26中发生的突变会导致斯克拉班-德达尔多夫综合征 (SKDEAS),影响CTLH E3无素结合酶复合体. 大多数突变会破坏复杂的组合和功能,为这种神经发育障碍提供了洞察力.
科学领域:
- 生物化学 生化学
- 遗传学 是一个遗传学.
- 神经科学是一个神经科学.
关键词:
GID/CTLH E3 泛素结合酶复合体在HBP1中,HBP1可能是HBP1.斯克迪亚斯 (SKDEAS) 是一个斯克拉班 - 德多夫综合征这就是WDR2626的功能.在YPEL5中,YPEL5就是YPEL5.更多相关视频
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