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...

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Xehetasun bibliografikoak
Egile nagusia: figshare admin karger (2628495) (author)
Beste egile batzuk: SarıYanartaş M. (22687652) (author), YayıcıKöken Ö. (22687655) (author), Ceylan A.C. (22687658) (author), Bozacı A.E. (22687661) (author), TuralKara T. (22687664) (author), Haspolat Ş. (22687667) (author)
Argitaratua: 2025
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