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SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation.

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dc.contributor.authorCascon Soriano, Alberto
dc.contributor.authorCebrián, A
dc.contributor.authorRuiz-Llorente, S
dc.contributor.authorTellería, D
dc.contributor.authorBenítez, J
dc.contributor.authorRobledo, M
dc.date.accessioned2025-01-17T15:29:29Z
dc.date.available2025-01-17T15:29:29Z
dc.date.issued2002-10
dc.description.peerreviewedSí
dc.description.tableofcontentsWe thank the patients participating in this study and the clinicians who provided blood samples and clinical information. We are also grateful for the technical assistance of Rocio Leton. This work was partially supported by the Fondo de Investigaciones Sanitarias project, FIS 00/0118. Alberto Cascon is a postdoctoral fellow of the Excmo Ayuntamiento de Madrid, Spain.
dc.format.number10
dc.format.pageE64
dc.format.volume39
dc.identifier.journalJ Med Genet
dc.identifier.pmchttps://pmc.ncbi.nlm.nih.gov/articles/PMC1734998/pdf/v039p00e64.pdf
dc.identifier.pubmedID12362046
dc.identifier.urihttps://hdl.handle.net/20.500.12105/26061
dc.language.isoeng
dc.publisherBMJ Publising Group
dc.relation.publisherversionhttp://doi: 10.1136/jmg.39.10.e64.
dc.repisalud.institucionCNIO
dc.repisalud.orgCNIOCNIO::Grupos de investigación::Grupo de Cáncer Endocrino Hereditario
dc.rights.accessRightsopen access
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectCOMPLEX-II GENE
dc.subjectENDOCRINE NEOPLASIA
dc.titleSDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation.
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublication610499dd-7ca3-4e9a-8b44-e5489f9212ab
relation.isAuthorOfPublication.latestForDiscovery610499dd-7ca3-4e9a-8b44-e5489f9212ab

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