The clinical picture of ERCC6L2 disease: from bone marrow failure to acute leukemia
dc.contributor.author | Hakkarainen, M | en_US |
dc.contributor.author | Kaaja, I | en_US |
dc.contributor.author | Douglas, SPM | en_US |
dc.contributor.author | Vulliamy, T | en_US |
dc.contributor.author | Dokal, I | en_US |
dc.contributor.author | Soulier, J | en_US |
dc.contributor.author | Larcher, L | en_US |
dc.contributor.author | de Latour, RP | en_US |
dc.contributor.author | Leblanc, T | en_US |
dc.contributor.author | de Fontbrune, FS | en_US |
dc.contributor.author | Siitonen, T | en_US |
dc.contributor.author | Lohi, O | en_US |
dc.contributor.author | Hellstrom-Lindberg, E | en_US |
dc.contributor.author | Barbany, G | en_US |
dc.contributor.author | Tesi, B | en_US |
dc.contributor.author | Shimamura, A | en_US |
dc.contributor.author | Beier, F | en_US |
dc.contributor.author | Jackson, S | en_US |
dc.contributor.author | Kuperman, AA | en_US |
dc.contributor.author | Zaccai, TF | en_US |
dc.contributor.author | Tamary, H | en_US |
dc.contributor.author | Mecucci, C | en_US |
dc.contributor.author | Capolsini, I | en_US |
dc.contributor.author | Jahnukainen, K | en_US |
dc.contributor.author | Salmenniemi, U | en_US |
dc.contributor.author | Niinimaki, R | en_US |
dc.contributor.author | Varilo, T | en_US |
dc.contributor.author | Kilpivaara, O | en_US |
dc.contributor.author | Wartiovaara-Kautto, U | en_US |
dc.date.accessioned | 2023-05-04T09:57:15Z | |
dc.date.available | 2023-02-27 | en_US |
dc.date.issued | 2023 | en_US |
dc.identifier.issn | 0006-4971 | en_US |
dc.identifier.uri | https://qmro.qmul.ac.uk/xmlui/handle/123456789/86173 | |
dc.format.extent | 2853 - 2866 | en_US |
dc.relation.ispartof | BLOOD | en_US |
dc.title | The clinical picture of ERCC6L2 disease: from bone marrow failure to acute leukemia | en_US |
dc.type | Article | |
dc.identifier.doi | 10.1182/blood.2022019425 | en_US |
pubs.author-url | https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:001021353100001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6a | en_US |
pubs.issue | 23 | en_US |
pubs.notes | Not known | en_US |
pubs.publication-status | Published | en_US |
pubs.volume | 141 | en_US |
qmul.funder | The genetic basis and pathophysiology of dyskeratosis congenita, aplastic anaemia, myelodysplasia and related disorders::Wellcome Trust | en_US |