P5709Hair and cutaneous phenotypes linked to Arrhythmogenic Cardiomyopathy caused by Desmoplakin haploinsufficiency: an additional disease marker
| dc.contributor.author | Castelletti, S | en_US |
| dc.contributor.author | Maruthappu, T | en_US |
| dc.contributor.author | Posafalvi, A | en_US |
| dc.contributor.author | Syrris, P | en_US |
| dc.contributor.author | O'Toole, EA | en_US |
| dc.contributor.author | Green, KJ | en_US |
| dc.contributor.author | Tinker, A | en_US |
| dc.contributor.author | McKenna, WJ | en_US |
| dc.contributor.author | Kelsell, DP | en_US |
| dc.date.accessioned | 2020-09-08T11:37:38Z | |
| dc.date.issued | 2018-08-01 | en_US |
| dc.identifier.issn | 0195-668X | en_US |
| dc.identifier.other | P5709 | |
| dc.identifier.uri | https://qmro.qmul.ac.uk/xmlui/handle/123456789/66852 | |
| dc.relation.ispartof | European Heart Journal | en_US |
| dc.title | P5709Hair and cutaneous phenotypes linked to Arrhythmogenic Cardiomyopathy caused by Desmoplakin haploinsufficiency: an additional disease marker | en_US |
| dc.title.alternative | Hair and cutaneous phenotypes linked to Arrhythmogenic Cardiomyopathy caused by Desmoplakin haploinsufficiency: an additional disease marker | en_US |
| dc.type | Article | |
| dc.identifier.doi | 10.1093/eurheartj/ehy566.p5709 | en_US |
| pubs.issue | suppl_1 | en_US |
| pubs.notes | Not known | en_US |
| pubs.volume | 39 | en_US |
| rioxxterms.funder | Default funder | en_US |
| rioxxterms.identifier.project | Default project | en_US |
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