Associated Papers
Neurodevelopmental Implications Underpinning Hereditary Spastic Paraplegia.
Zhi Y et al.
Cns Neuroscience & Therapeutics, 2025
39932116 (PubMed )
Supplement: CNS-31-e70260-s001.xlsx › SPG57
Novel TFG mutation causes autosomal-dominant spastic paraplegia and defects in autophagy.
Xu L et al.
Journal of Medical Genetics, 2024
Recent advances in novel mutation genes of Parkinson's disease.
Yang J et al.
Journal of Neurology, 2023
Parkinson's Disease, Parkinsonisms, and Mitochondria: the Role of Nuclear and Mitochondrial DNA.
Legati A et al.
Current Neurology and Neuroscience Reports, 2023
A novel TFG variant of uncertain significance in amyotrophic lateral sclerosis: A case report and review of literature.
Dhakal B et al.
Annals of Medicine and Surgery (2012), 2022
Mutation Screening of TFG in α-Synucleinopathy and Amyotrophic Lateral Sclerosis.
Li C et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2022
A Novel TFG Mutation in a Korean Family with α-Synucleinopathy and Amyotrophic Lateral Sclerosis.
Yoo D et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2022
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