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CALR-mutated patients with low allele burden represent a specific subtype of essential thrombocythemia: A study on behalf of FIM and GBMHM.

dc.rights.licenseopenen_US
dc.contributor.authorAUBIN, Laura
dc.contributor.authorVILAS BOAS, Rúben
dc.contributor.authorDALTRO DE OLIVEIRA, Rafael
dc.contributor.authorLE BRUN, Valoris
dc.contributor.authorDIVOUX, Marion
dc.contributor.authorREY, Jérôme
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorMANSIER, Olivier
dc.contributor.authorIANOTTO, Jean-Christophe
dc.contributor.authorPASTORET, Cédric
dc.contributor.authorDESMARES, Anne
dc.contributor.authorMURATI, Anne
dc.contributor.authorDE MAS, Véronique
dc.contributor.authorTAVITIAN, Suzanne
dc.contributor.authorGIRODON, François
dc.contributor.authorSORET DULPHY, Juliette
dc.contributor.authorMASLAH, Nabih
dc.contributor.authorGONCALVES MONTEIRO, Valérie
dc.contributor.authorBOYER, Françoise
dc.contributor.authorORVAIN, Corentin
dc.contributor.authorRANTA, Dana
dc.contributor.authorCAYSSIALS, Émilie
dc.contributor.authorLE CLECH, Lenaig
dc.contributor.authorNICOL, Christophe
dc.contributor.authorROTTIER, Camille
dc.contributor.authorBOTIN LOPEZ, Teresa
dc.contributor.authorCASTEL, Brice
dc.contributor.authorRISPAL, Patrick
dc.contributor.authorBEZIAT, Guillaume
dc.contributor.authorBESCOND, Charles
dc.contributor.authorLARIBI, Kamel
dc.contributor.authorBENAJIBA, Lina
dc.contributor.authorUGO, Valérie
dc.contributor.authorLIPPERT, Eric
dc.contributor.authorCOTTIN, Laurane
dc.contributor.authorLUQUE PAZ, Damien
dc.date.accessioned2024-03-25T15:02:13Z
dc.date.available2024-03-25T15:02:13Z
dc.date.issued2024-02-25
dc.identifier.issn1096-8652en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/188963
dc.description.abstractEnA low allele burden (i.e., <20%) of the CALR driver mutation is found in 10.8% of CALR-mutated MPNs, mostly in essential thrombocythemia, and correlates with a milder phenotype and a more indolent evolution compared to patients with an allele burden ≥20%.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.title.enCALR-mutated patients with low allele burden represent a specific subtype of essential thrombocythemia: A study on behalf of FIM and GBMHM.
dc.title.alternativeAm J Hematolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1002/ajh.27265en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed38404143en_US
bordeaux.journalAmerican Journal of Hematologyen_US
bordeaux.hal.laboratoriesBiologie des maladies cardiovasculaires (BMC) - UMR 1034en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04520328
hal.version1
hal.date.transferred2024-03-25T15:02:17Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=American%20Journal%20of%20Hematology&amp;rft.date=2024-02-25&amp;rft.eissn=1096-8652&amp;rft.issn=1096-8652&amp;rft.au=AUBIN,%20Laura&amp;VILAS%20BOAS,%20R%C3%BAben&amp;DALTRO%20DE%20OLIVEIRA,%20Rafael&amp;LE%20BRUN,%20Valoris&amp;DIVOUX,%20Marion&amp;rft.genre=article


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