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dc.contributor.authorTabernero, María Dolores
dc.contributor.authorJara Acevedo, María 
dc.contributor.authorNieto Librero, Ana Belén 
dc.contributor.authorRodríguez Caballero, María Arantzazu 
dc.contributor.authorOtero Rodríguez, Álvaro 
dc.contributor.authorSousa, Pablo
dc.contributor.authorGonçalves Estella, Jesús María 
dc.contributor.authorDomingues, Patricia H.
dc.contributor.authorOrfao de Matos Correia e Vale, José Alberto 
dc.date.accessioned2024-04-11T16:36:47Z
dc.date.available2024-04-11T16:36:47Z
dc.date.issued2013
dc.identifier.citationTabernero, M., Jara-Acevedo, M., Nieto, A. B., Caballero, A. R., Otero, Á., Sousa, P., Gonçalves, J., Domingues, P. H., & Orfao, A. (2013). Association between mutation of the NF2 gene and monosomy 22 in menopausal women with sporadic meningiomas. BMC Medical Genetics, 14(1). https://doi.org/10.1186/1471-2350-14-114es_ES
dc.identifier.issn1471-2350
dc.identifier.urihttp://hdl.handle.net/10366/157296
dc.description.abstract[EN] Meningioma was the first solid tumor shown to contain a recurrent genetic alteration e.g. monosomy 22/del(22q), NF2 being the most relevant gene involved. Although monosomy 22/del(22q) is present in half of all meningiomas, and meningiomas frequently carry NF2 mutations, no study has been reported so far in which both alterations are simultaneously assessed and correlated with the features of the disease.es_ES
dc.language.isoenges_ES
dc.publisherBioMed Centrales_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectMutationes_ES
dc.subjectNF2 genees_ES
dc.subjectSporadic meningiomases_ES
dc.subjectMonosomy 22es_ES
dc.subjectMenopausal womenes_ES
dc.titleAssociation between mutation of the NF2gene and monosomy 22 in menopausal women with sporadic meningiomases_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://bmcmedgenet.biomedcentral.com/articles/10.1186/1471-2350-14-114es_ES
dc.subject.unesco3201 Ciencias Clínicases_ES
dc.identifier.doi10.1186/1471-2350-14-114
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.journal.titleBMC Medical Geneticses_ES
dc.volume.number14es_ES
dc.issue.number1es_ES
dc.page.initial114es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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