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A genetic study of Wilson's disease in the United Kingdom.
Coffey AJ, Durkie M, Hague S, McLay K, Emmerson J, Lo C, Klaffke S, Joyce CJ, Dhawan A, Hadzic N, Mieli-Vergani G, Kirk R, Elizabeth Allen K, Nicholl D, Wong S, Griffiths W, Smithson S, Giffin N, Taha A, Connolly S, Gillett GT, Tanner S, Bonham J, Sharrack B, Palotie A, Rattray M, Dalton A, Bandmann O. Coffey AJ, et al. Among authors: bandmann o. Brain. 2013 May;136(Pt 5):1476-87. doi: 10.1093/brain/awt035. Epub 2013 Mar 21. Brain. 2013. PMID: 23518715 Free PMC article.
Mitochondrial function and morphology are impaired in parkin-mutant fibroblasts.
Mortiboys H, Thomas KJ, Koopman WJ, Klaffke S, Abou-Sleiman P, Olpin S, Wood NW, Willems PH, Smeitink JA, Cookson MR, Bandmann O. Mortiboys H, et al. Among authors: bandmann o. Ann Neurol. 2008 Nov;64(5):555-65. doi: 10.1002/ana.21492. Ann Neurol. 2008. PMID: 19067348 Free PMC article.
Animal models of Wilson disease.
Reed E, Lutsenko S, Bandmann O. Reed E, et al. Among authors: bandmann o. J Neurochem. 2018 Aug;146(4):356-373. doi: 10.1111/jnc.14323. Epub 2018 Jun 26. J Neurochem. 2018. PMID: 29473169 Free PMC article. Review.
147 results