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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, G; Houlden, HH; Kalmar, B; Greensmith, L; Reilly, MM; (2012) A novel p.glu175x premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2. In: (Proceedings) United Kingdom Neuromuscular Translational Research Conference. (pp. S21-S21). PERGAMON-ELSEVIER SCIENCE LTD

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Type: Proceedings paper
Title: A novel p.glu175x premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2
Event: United Kingdom Neuromuscular Translational Research Conference
Location: Newcastle upon Tyne, ENGLAND
Dates: 22 March 2012 - 23 March 2012
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences, Neurosciences & Neurology
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/1346588
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