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Annals of Neurology, ISSN 0364-5134, 06/2016, Volume 79, Issue 6, pp. 983 - 990
Journal Article
Basal Ganglia, ISSN 2210-5336, 05/2017, Volume 8, pp. 21 - 21
(2) German Center of Neurodegenerative Diseases (DZNE), Eberhard-Karls-University, Tu bingen, Germany 
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 12/2016, Volume 87, Issue 12, pp. e1 - e1
Over 30 diseases are caused by expansion of microsatellite sequences; nine by expanded CAG tracts encoding polyglutamines. These include Huntington's disease... 
Journal Article
Annals of Neurology, ISSN 0364-5134, 07/2016, Volume 80, Issue 1, pp. 170 - 171
Journal Article
Annals of Neurology, ISSN 0364-5134, 07/2016, Volume 80, Issue 1, pp. 170 - 171
Journal Article
Annals of Neurology, ISSN 0364-5134, 07/2016, Volume 80, Issue 1, p. 170
Journal Article
Annals of Neurology, ISSN 0364-5134, 07/2016, Volume 80, Issue 1, pp. 170 - 171
Journal Article
Annals of Neurology, ISSN 0364-5134, 2016
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 11/2018, Volume 89, Issue 11, pp. 1226 - 1227
Interestingly, SCA6 expanded alleles lie within the normal range of repeat sizes for all other polyQ diseases, below their respective pathogenic thresholds... 
disease modifying factors | polyglutamine diseases | Spinocerebellar ataxia type 6 | trinucleotide repeat expansions | repeat interruptions | SURGERY | PSYCHIATRY | CLINICAL NEUROLOGY | Brain research | Disease | Funding | Ataxia | Genetic testing | Mutation | DNA repair | Deoxyribonucleic acid--DNA | University colleges | 1506 | PostScript
Journal Article
by Meyer, E and Carss, K.J and Rankin, J and Nichols, J.M and Grozeva, D and Joseph, A.P and Mencacci, N.E and Papaneou, A and Ng, J and Barral, S and Ngoh, A and Ben-Pazi, H and Willemsen, M.A and Arkadir, D and Barnicoat, A and Bergman, H and Bhate, S and Boys, A and Darin, N and Foulds, N and Gutowski, N and Hills, A and Houlden, H and Hurst, J.A and Israel, Z and Kaminska, M and Limousin, P and Lumsden, D and McKee, S and Misra, S and Mohammed, S.S and Nakou, V and Nicolai, J and Nilsson, M and Pall, H and Peall, K.J and Peters, G.B and Prabhakar, P and Reuter, M.S and Rump, P and Segel, R and Sinnema, M and Smith, M and Turnpenny, P and White, S.M and Wieczorek, D and Wiethoff, S and Wilson, B.T and Winter, G and Wragg, C and Pope, S and Heales, S.J and Morrogh, D and Pittman, A and Carr, L.J and Perez-Duenas, B and Lin, J.P and Reis, A and Gahl, W.A and Toro, C and Bhatia, K.P and Wood, N.W and Kamsteeg, E.J and Chong, W.K and Gissen, P and Topf, M and Dale, R.C and Chubb, J.R and Raymond, F.L and Kurian, M.A and NIHR BioResource Rare and Deciphering Dev Disorders Study and UK10K Consortium and Deciphering Developmental Disorders Study and NIHR BioResource Rare Diseases Consortium and Sahlgrenska akademin and Institute of Clinical Sciences, Section for the Health of Women and Children, Department of Pediatrics and Göteborgs universitet and Gothenburg University and Institutionen för kliniska vetenskaper, sektionen för kvinnors och barns hälsa, Avdelningen för pediatrik and Sahlgrenska Academy
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 2, pp. 223 - 237
Journal Article
Stem Cells International, ISSN 1687-966X, 2016, Volume 2016, pp. 8291260 - 14
Journal Article