Items where authors include "Rossor, A.M."

Article

Maroofian, R. orcid.org/0000-0001-6763-1542, Sarraf, P., O’Brien, T.J. et al. (29 more authors) (2024) RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity. Brain, 147 (7). pp. 2334-2343. ISSN 0006-8950

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

Zis, P., Reilly, M.M., Rao, D.G. et al. (3 more authors) (2017) A novel mutation in the FGD4 gene causing Charcot-Marie-Tooth disease. Journal of the Peripheral Nervous System, 22 (3). pp. 224-225. ISSN 1085-9489