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:
| Main Author: | |
|---|---|
| Other Authors: | , , , , , |
| Published: |
2025
|
| Subjects: | |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|