Items where authors include "Nemeth, A.H."

Article

Fasham, J., Rankin, J., Schot, R. et al. (40 more authors) (2026) Palindrome-mediated 16p13.3 triplications cause a recognizable neurodegenerative disorder with ataxia. The American Journal of Human Genetics, 113 (1). pp. 221-233. ISSN 0002-9297

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

Vezyroglou, A., Akilapa, R., Barwick, K. et al. (26 more authors) (2022) The phenotypic continuum of ATPLA3-related disorders. Neurology, 99 (14). e1511-e1526. ISSN 0028-3878