Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Reference4 articles.
1. Matilla-Dueñas A, Sánchez I, Corral-Juan M, Dávalos A, Alvarez R, Latorre P. Cellular and molecular pathways triggering neurodegeneration in the spinocerebellar ataxias. Cerebellum Lond Engl. 2010;9:148–66.
2. Klivényi P, Horváth Z, Vécsei L. A spinocerebellaris ataxiák klinikuma és diagnosztikája [Clinical features and diagnosis of spinocerebellar ataxia]. Ideggyogyaszati Sz. 2004;57:11–22.
3. Wang JL, Yang X, Xia K, et al. TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing. Brain. 2010;133:3510–8.
4. Manini A, Bocci T, Migazzi A, et al. A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutation. BMC Neurol. 2020;20:408.