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Semi-dominant mutations in MFN2-related neuropathy and implications for genetic counselling

Tomaselli, PJ; Rossor, AM; Polke, JM; Poh, R; Blake, J; Reilly, MM; (2016) Semi-dominant mutations in MFN2-related neuropathy and implications for genetic counselling. Journal of the Peripheral Nervous System , 21 (1) pp. 52-54. 10.1111/jns.12155. Green open access

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Type: Article
Title: Semi-dominant mutations in MFN2-related neuropathy and implications for genetic counselling
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1111/jns.12155
Publisher version: http://dx.doi.org/10.1111/jns.12155
Language: English
Additional information: This is the peer reviewed version of the following article: Tomaselli, PJ; Rossor, AM; Polke, JM; Poh, R; Blake, J; Reilly, MM; (2016) Semi-dominant mutations in MFN2-related neuropathy and implications for genetic counselling. Journal of the Peripheral Nervous System, 21 (1) pp. 52-54, which has been published in final form at: http://dx.doi.org/10.1111/jns.12155. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving (http://olabout.wiley.com/WileyCDA/Section/id-820227.html#terms).
Keywords: Charcot-Marie-Tooth disease, Mitofusin 2, dominant, recessive, semi-dominant
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 > Department of Neuromuscular Diseases
URI: https://discovery.ucl.ac.uk/id/eprint/1479602
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