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De novo KCNA2 mutations cause hereditary spastic paraplegia

Manole, A; Mannikko, R; Hanna, MG; Kullmann, DM; Houlden, H; (2017) De novo KCNA2 mutations cause hereditary spastic paraplegia. [Letter]. Annals of Neurology , 81 (2) pp. 326-328. 10.1002/ana.24866. Green open access

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Type: Article
Title: De novo KCNA2 mutations cause hereditary spastic paraplegia
Open access status: An open access version is available from UCL Discovery
DOI: 10.1002/ana.24866
Publisher version: http://doi.org/10.1002/ana.24866
Language: English
Additional information: © 2016 American Neurological Association. This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences, Neurosciences & Neurology, EPILEPTIC ENCEPHALOPATHY
UCL classification: UCL
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 > Clinical and Experimental Epilepsy
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: https://discovery.ucl.ac.uk/id/eprint/1534356
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