Associated Papers
Missense variant in TTBK2 kinase domain causes loss of function and impaired protein phosphorylation.
Felício D et al.
Scientific Reports, 2025
Spinocerebellar ataxia type 11 (SCA11): TTBK2 variants, functions and associated disease mechanisms.
Felício D et al.
Cerebellum (london, England), 2024
Spinocerebellar ataxia type 11 (SCA11): An update.
Gong Z et al.
The European Journal of Neuroscience, 2023
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