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Clinical and genetic characterisation of hereditary sensory neuropathy type 1 caused by mutations in SPTLC2

Murphy, SM; Laura, M; Ernst, D; Liu, Y-T; Blake, J; Donaghy, M; Winer, J; ... Reilly, MM; + view all (2012) Clinical and genetic characterisation of hereditary sensory neuropathy type 1 caused by mutations in SPTLC2. In: (Proceedings) United Kingdom Neuromuscular Translational Research Conference. (pp. S19-S19). PERGAMON-ELSEVIER SCIENCE LTD

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Type: Proceedings paper
Title: Clinical and genetic characterisation of hereditary sensory neuropathy type 1 caused by mutations in SPTLC2
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
URI: http://discovery.ucl.ac.uk/id/eprint/1346622
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