Associated Papers
Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia.
Zhu R et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2025
CPT1C-related Spastic-Ataxia: Expanding the clinical spectrum of SPG73.
Ganguly J et al.
Parkinsonism & Related Disorders, 2025
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