UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

The inherited ataxias: Genetic heterogeneity, mutation databases, and future directions in research and clinical diagnostics

Hersheson, J; Haworth, A; Houlden, H; (2012) The inherited ataxias: Genetic heterogeneity, mutation databases, and future directions in research and clinical diagnostics. HUMAN MUTATION , 33 (9) pp. 1324-1332. 10.1002/humu.22132.

Full text not available from this repository.
Type: Article
Title: The inherited ataxias: Genetic heterogeneity, mutation databases, and future directions in research and clinical diagnostics
DOI: 10.1002/humu.22132
Keywords: Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, ataxia, mutation database, neurogenetics, next-generation sequencing, DOMINANT CEREBELLAR ATAXIAS, KINASE-C-GAMMA, EPISODIC ATAXIA, SPINOCEREBELLAR ATAXIAS, CHANNEL GENE, PHENOTYPE, PATHOGENESIS, TYPE-14
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 > Department of Neuromuscular Diseases
URI: http://discovery.ucl.ac.uk/id/eprint/1349543
Downloads since deposit
0Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item