Associated Papers
Missense variant in TTBK2 kinase domain causes loss of function and impaired protein phosphorylation.
Felício D et al.
Scientific Reports, 2025
41422144 (PubMed )
Supplement: 41598_2025_32288_MOESM2_ESM.docx
Spinocerebellar ataxia type 11 (SCA11): TTBK2 variants, functions and associated disease mechanisms.
Felício D et al.
Cerebellum (london, England), 2024
NGS in Hereditary Ataxia: When Rare Becomes Frequent.
Galatolo D et al.
International Journal of Molecular Sciences, 2021
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