Supplementary Material for: CAPOS and Beyond: ATP1A3 Variants in Pediatric Movement Disorders: Case Reports
Introduction: ATP1A3-related disorders encompass a clinically heterogeneous spectrum that includes previously defined dominantly inherited phenotypes such as Alternating Hemiplegia of Childhood (AHC), Rapid-Onset Dystonia-Parkinsonism (RDP), and cerebellar ataxia, areflexia, pes cavus, optic atrophy...
Saved in:
| 主要作者: | |
|---|---|
| 其他作者: | , , , , , |
| 出版: |
2025
|
| 主题: | |
| 标签: |
添加标签
没有标签, 成为第一个标记此记录!
|