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Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/184941
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dc.contributor.authorMoulin, Philippe-
dc.contributor.authorDufour, Robert-
dc.contributor.authorAverna, Maurizio-
dc.contributor.authorArca, Marcello-
dc.contributor.authorCefalù, Angelo B.-
dc.contributor.authorNoto, Davide-
dc.contributor.authorD'Erasmo, Laura-
dc.contributor.authorDi Costanzo, Alessia-
dc.contributor.authorMarçais, Christophe-
dc.contributor.authorAlvarez-Sala Walther, Luis Antonio-
dc.contributor.authorBanach, Maciej-
dc.contributor.authorBorén, Jan-
dc.contributor.authorCramb, Robert-
dc.contributor.authorGouni-Berthold, Ionna-
dc.contributor.authorHughes, Elizabeth-
dc.contributor.authorJohnson, Colin-
dc.contributor.authorPintó Sala, Xavier-
dc.contributor.authorReiner, eljko-
dc.contributor.authorRoeters Van Lennep, Jeanine-
dc.contributor.authorSoran, Handrean-
dc.contributor.authorStefanutti, Claudia-
dc.contributor.authorStroes, Erik-
dc.contributor.authorBruckert, Eric-
dc.date.accessioned2022-04-11T16:08:42Z-
dc.date.available2022-04-11T16:08:42Z-
dc.date.issued2018-10-27-
dc.identifier.issn2352-3409-
dc.identifier.urihttp://hdl.handle.net/2445/184941-
dc.description.abstractData presented in this article are supplementary material to our article entitled "Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): expert panel recom mendations and proposal of an "FCS Score" (Moulin et al., 2018, in press). The data describe the genotypes of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicro naemia syndrome (MCS), from the validation and replication cohorts.-
dc.format.extent3 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1016/j.dib.2018.10.125-
dc.relation.ispartofData in Brief, 2018, vol. 21, p. 1334-1336-
dc.relation.urihttps://doi.org/10.1016/j.dib.2018.10.125-
dc.rightscc-by (c) Moulin, Philippe et al., 2018-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.sourceArticles publicats en revistes (Ciències Clíniques)-
dc.subject.classificationMalalties hereditàries-
dc.subject.classificationDiagnòstic-
dc.subject.classificationMalalties rares-
dc.subject.otherGenetic diseases-
dc.subject.otherDiagnosis-
dc.subject.otherRare diseases-
dc.titleCharacterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): establishment of an FCS clinical diagnostic score-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec688119-
dc.date.updated2022-04-11T16:08:42Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Ciències Clíniques)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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