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.
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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-pp.ucl.ac.uk/id/eprint/1479602 |
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