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Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma.

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dc.contributor.authorPertesi, Maroulio
dc.contributor.authorVallée, Maxime
dc.contributor.authorWei, Xiaomu
dc.contributor.authorRevuelta, Maria V
dc.contributor.authorGalia, Perrine
dc.contributor.authorDemangel, Delphine
dc.contributor.authorOliver, Javier
dc.contributor.authorFoll, Matthieu
dc.contributor.authorChen, Siwei
dc.contributor.authorPerrial, Emeline
dc.contributor.authorGarderet, Laurent
dc.contributor.authorCorre, Jill
dc.contributor.authorLeleu, Xavier
dc.contributor.authorBoyle, Eileen M
dc.contributor.authorDecaux, Olivier
dc.contributor.authorRodon, Philippe
dc.contributor.authorKolb, Brigitte
dc.contributor.authorSlama, Borhane
dc.contributor.authorMineur, Philippe
dc.contributor.authorVoog, Eric
dc.contributor.authorLe Bris, Catherine
dc.contributor.authorFontan, Jean
dc.contributor.authorMaigre, Michel
dc.contributor.authorBeaumont, Marie
dc.contributor.authorAzais, Isabelle
dc.contributor.authorSobol, Hagay
dc.contributor.authorVignon, Marguerite
dc.contributor.authorRoyer, Bruno
dc.contributor.authorPerrot, Aurore
dc.contributor.authorFuzibet, Jean-Gabriel
dc.contributor.authorDorvaux, Véronique
dc.contributor.authorAnglaret, Bruno
dc.contributor.authorCony-Makhoul, Pascale
dc.contributor.authorBerthou, Christian
dc.contributor.authorDesquesnes, Florence
dc.contributor.authorPegourie, Brigitte
dc.contributor.authorLeyvraz, Serge
dc.contributor.authorMosser, Laurent
dc.contributor.authorFrenkiel, Nicole
dc.contributor.authorAugeul-Meunier, Karine
dc.contributor.authorLeduc, Isabelle
dc.contributor.authorLeyronnas, Cécile
dc.contributor.authorVoillat, Laurent
dc.contributor.authorCasassus, Philippe
dc.contributor.authorMathiot, Claire
dc.contributor.authorCheron, Nathalie
dc.contributor.authorPaubelle, Etienne
dc.contributor.authorMoreau, Philippe
dc.contributor.authorBignon, Yves-Jean
dc.contributor.authorJoly, Bertrand
dc.contributor.authorBourquard, Pascal
dc.contributor.authorCaillot, Denis
dc.contributor.authorNaman, Hervé
dc.contributor.authorRigaudeau, Sophie
dc.contributor.authorMarit, Gérald
dc.contributor.authorMacro, Margaret
dc.contributor.authorLambrecht, Isabelle
dc.contributor.authorCliquennois, Manuel
dc.contributor.authorVincent, Laure
dc.contributor.authorHelias, Philippe
dc.contributor.authorAvet-Loiseau, Hervé
dc.contributor.authorMoreno, Victor
dc.contributor.authorReis, Rui Manuel
dc.contributor.authorVarkonyi, Judit
dc.contributor.authorKruszewski, Marcin
dc.contributor.authorVangsted, Annette Juul
dc.contributor.authorJurczyszyn, Artur
dc.contributor.authorZaucha, Jan Maciej
dc.contributor.authorSainz, Juan
dc.contributor.authorKrawczyk-Kulis, Malgorzata
dc.contributor.authorWątek, Marzena
dc.contributor.authorPelosini, Matteo
dc.contributor.authorIskierka-Jażdżewska, Elzbieta
dc.contributor.authorGrząśko, Norbert
dc.contributor.authorMartinez-Lopez, Joaquin
dc.contributor.authorJerez, Andrés
dc.contributor.authorCampa, Daniele
dc.contributor.authorBuda, Gabriele
dc.contributor.authorLesueur, Fabienne
dc.contributor.authorDudziński, Marek
dc.contributor.authorGarcía-Sanz, Ramón
dc.contributor.authorNagler, Arnon
dc.contributor.authorRymko, Marcin
dc.contributor.authorJamroziak, Krzysztof
dc.contributor.authorButrym, Aleksandra
dc.contributor.authorCanzian, Federico
dc.contributor.authorObazee, Ofure
dc.contributor.authorNilsson, Björn
dc.contributor.authorKlein, Robert J
dc.contributor.authorLipkin, Steven M
dc.contributor.authorMcKay, James D
dc.contributor.authorDumontet, Charles
dc.date.accessioned2024-02-10T20:01:12Z
dc.date.available2024-02-10T20:01:12Z
dc.date.issued2019-04-09
dc.format.number9es_ES
dc.format.page2324-2330es_ES
dc.format.volume33es_ES
dc.identifier.doi10.1038/s41375-019-0452-6
dc.identifier.e-issn1476-5551es_ES
dc.identifier.journalLeukemiaes_ES
dc.identifier.otherhttp://hdl.handle.net/10668/13806
dc.identifier.pubmedID30967618es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/17844
dc.language.isoeng
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshExome
dc.subject.meshExosome Multienzyme Ribonuclease Complex
dc.subject.meshFemale
dc.subject.meshGenetic Predisposition to Disease
dc.subject.meshGerm-Line Mutation
dc.subject.meshHumans
dc.subject.meshMultiple Myeloma
dc.subject.meshPedigree
dc.subject.meshExome Sequencing
dc.titleExome sequencing identifies germline variants in DIS3 in familial multiple myeloma.
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublication9b25aa8e-597b-43e0-90d0-6d3846974c12
relation.isAuthorOfPublication.latestForDiscovery9b25aa8e-597b-43e0-90d0-6d3846974c12

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