UCL Discovery

Koutsis, G; Karadima, G; Pandraud, A; Sweeney, MG; Paudel, R; Houlden, H; Wood, NW; Koutsis, G; Karadima, G; Pandraud, A; Sweeney, MG; Paudel, R; Houlden, H; Wood, NW; Panas, M; - view fewer (2012) Genetic screening of Greek patients with Huntington's disease phenocopies identifies an SCA8 expansion. JOURNAL OF NEUROLOGY , 259 (9) pp. 1874-1878. 10.1007/s00415-012-6430-9.

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Type:	Article
Title:	Genetic screening of Greek patients with Huntington's disease phenocopies identifies an SCA8 expansion
DOI:	10.1007/s00415-012-6430-9
Keywords:	Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, Huntington disease phenocopies, Huntington's disease-like syndromes, Spinocerebellar ataxia, SCA8, SPINOCEREBELLAR ATAXIA, BIDIRECTIONAL EXPRESSION, TRINUCLEOTIDE REPEAT, MUTATION, PHENOTYPE, TYPE-8, FAMILY
UCL classification:	UCL > Provost and Vice Provost Offices UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Clinical and Movement Neurosciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Department of Neuromuscular Diseases
URI:	http://discovery.ucl.ac.uk/id/eprint/1339374

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