Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): establishment of an FCS clinical diagnostic score

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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.date.updated2022-04-11T16:08:42Z
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.identifier.idgrec688119
dc.identifier.issn2352-3409
dc.identifier.urihttps://hdl.handle.net/2445/184941
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.accessRightsinfo:eu-repo/semantics/openAccess
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

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