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Sequencing analysis of the spinal bulbar muscular atrophy CAG expansion reveals absence of repeat interruptions

Fratta, P; Collins, T; Pemble, S; Nethisinghe, S; Devoy, A; Giunti, P; Sweeney, MG; ... Fisher, EMC; + view all (2014) Sequencing analysis of the spinal bulbar muscular atrophy CAG expansion reveals absence of repeat interruptions. NEUROBIOLOGY OF AGING , 35 (2) 10.1016/j.neurobiolaging.2013.07.015.

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Type: Article
Title: Sequencing analysis of the spinal bulbar muscular atrophy CAG expansion reveals absence of repeat interruptions
DOI: 10.1016/j.neurobiolaging.2013.07.015
Keywords: Science & Technology, Life Sciences & Biomedicine, Geriatrics & Gerontology, Neurosciences, Neurosciences & Neurology, GERIATRICS & GERONTOLOGY, NEUROSCIENCES, Kennedy's disease, Spinal bulbar muscular atrophy, CAG, Trinucleotide, Interruptions, SPINOCEREBELLAR ATAXIA TYPE-1, TRINUCLEOTIDE REPEAT, GENE, DISEASE, SCA1
UCL classification: UCL > School of Life and Medical Sciences
UCL > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > School of Life and Medical Sciences > Faculty of Brain Sciences > Institute of Neurology
UCL > School of Life and Medical Sciences > Faculty of Brain Sciences > Institute of Neurology > Molecular Neuroscience
UCL > School of Life and Medical Sciences > Faculty of Brain Sciences > Institute of Neurology > Neurodegenerative Diseases
URI: http://discovery.ucl.ac.uk/id/eprint/1408197
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