Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations
| dc.contributor.author | Lynch, DS | en_US |
| dc.contributor.author | Loh, SHY | en_US |
| dc.contributor.author | Harley, J | en_US |
| dc.contributor.author | Noyce, AJ | en_US |
| dc.contributor.author | Martins, LM | en_US |
| dc.contributor.author | Wood, NW | en_US |
| dc.contributor.author | Houlden, H | en_US |
| dc.contributor.author | Plun-Favreau, H | en_US |
| dc.date.accessioned | 2018-02-12T11:59:24Z | |
| dc.date.available | 2017-07-05 | en_US |
| dc.date.issued | 2017-10 | en_US |
| dc.date.submitted | 2017-12-16T17:37:06.175Z | |
| dc.identifier.uri | http://qmro.qmul.ac.uk/xmlui/handle/123456789/32250 | |
| dc.description.sponsorship | Leonard Wolfson Experimental Neurology Centre, the Medical Research Council, and the Wellcome Trust. | en_US |
| dc.format.extent | e188 - e188 | en_US |
| dc.language.iso | en | en_US |
| dc.relation.ispartof | Neurology Genetics | en_US |
| dc.title | Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations | en_US |
| dc.type | Article | |
| dc.rights.holder | © 2017 The Author(s) | |
| dc.rights.holder | CC BY 4.0 | |
| dc.identifier.doi | 10.1212/NXG.0000000000000188 | en_US |
| pubs.issue | 5 | en_US |
| pubs.notes | No embargo | en_US |
| pubs.publication-status | Published | en_US |
| pubs.volume | 3 | en_US |
| dcterms.dateAccepted | 2017-07-05 | en_US |
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