Manole, A, Jaunmuktane, Z, Hargreaves, IP, Ludtmann, MHR, Salpietro, V, Bello, OD, Pope, S, Pandraud, A, Horga, A, Scalco, RS, Li, A, Ashokkumar, B, Lourenco, CM, Heales, S, Horvath, R, Chinnery, PF, Toro, C, Singleton, AB, Jacques, TS, Abramov, AY et al, Muntoni, F, Hanna, MG, Reilly, MM, Revesz, T, Kullmann, DM, Jepson, JEC and Houlden, H (2017) Clinical, pathological and functional characterization of riboflavin-responsive neuropathy. Brain, 140 (11). pp. 2820-2837. ISSN 1460-2156

Balreira, A, Boczonadi, V, Barca, E, Pyle, A, Bansagi, B, Appleton, M, Graham, C, Hargreaves, IP, Rasic, VM, Lochmueller, H, Griffin, H, Taylor, RW, Naini, A, Chinnery, PF, Hirano, M, Quinzii, CM and Horvath, R (2014) ANO10 mutations cause ataxia and coenzyme Q(10) deficiency. Journal of Neurology, 261 (11). pp. 2192-2198. ISSN 0340-5354

Wilding, CS, Cadwell, K, Tawn, EJ, Relton, CL, Taylor, GA, Chinnery, PF and Turnbull, DM (2006) Mitochondrial DNA mutations in individuals occupationally exposed to ionizing radiation. RADIATION RESEARCH, 165 (2). pp. 202-207. ISSN 0033-7587