第二个RUBCN变异与性脑病和神经发育迟缓相关
Lodin-Pasquier Magalie1, Capri Yline2, Patat Olivier3
1Department of Genetics, APHP-Robert Debré University Hospital, Paris, France.
American journal of medical genetics. Part A
|November 9, 2024
概括
在RUBCN基因中,一种新的拼接变异通过破坏Rubicon同理学领域,导致儿童发作的性脑病变. 这一发现扩大了神经发育障碍的已知遗传原因.
科学领域:
- 遗传学 是一个遗传学.
- 神经科学是一个神经科学.
- 分子生物学分子生物学
背景情况:
- 该RUBCN基因编码Rubicon,这是一个负面调节大自的蛋白质.
- 在RUBCN的致病变体已与脊髓小脑动症自体递归15相关.
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