Reply to letter to the editor by De Michele et al
- 6 February 2020
- journal article
- letter
- Published by Springer Science and Business Media LLC in neurogenetics
- Vol. 21 (2), 147
- https://doi.org/10.1007/s10048-020-00604-7
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Cerebellar cognitive-affective syndrome preceding ataxia associated with complex extrapyramidal features in a Turkish SCA48 familyneurogenetics, 2020
- The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian familiesEuropean Journal of Neurology, 2019
- Spinocerebellar ataxia 48 presenting with ataxia associated with cognitive, psychiatric, and extrapyramidal features: A report of two Italian familiesParkinsonism & Related Disorders, 2019
- Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48)Neurology, 2018