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A novel p.Glu175X premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2

Rossor, AM; Davidson, GL; Blake, J; Polke, JM; Murphy, SM; Houlden, H; Innes, A; ... Reilly, MM; + view all (2012) A novel p.Glu175X premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2. JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM , 17 (2) pp. 201-205. 10.1111/j.1529-8027.2012.00400.x.

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Type: Article
Title: A novel p.Glu175X premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2
DOI: 10.1111/j.1529-8027.2012.00400.x
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences, Neurosciences & Neurology, Charcot-Marie-Tooth disease, distal hereditary motor neuropathy, HSP27 heat shock proteins, HEREDITARY MOTOR NEUROPATHY, MARIE-TOOTH-DISEASE, HSPB1, DOMINANT
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
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > ION Central Administration
URI: http://discovery.ucl.ac.uk/id/eprint/1356674
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