Items where authors include "Dominik, N."

Article

Currò, R., Dominik, N., Facchini, S. et al. (155 more authors) (2024) Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease. Brain, 147 (5). pp. 1887-1898. ISSN 0006-8950

Hadjivassiliou, M. orcid.org/0000-0003-2542-8954, Currò, R., Beauchamp, N. et al. (6 more authors) (2024) Can CANVAS due to RFC1 biallelic expansions present with pure ataxia? Journal of Neurology, Neurosurgery & Psychiatry, 95 (2). pp. 171-174. ISSN 0022-3050

Saida, K., Maroofian, R., Sengoku, T. et al. (84 more authors) (2023) Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals. Genetics in Medicine, 25 (1). pp. 90-102. ISSN 1098-3600