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

Maurizio Averna, Angelo Baldassare Cefalu', Davide Noto, Maciej Banach, Laura D'Erasmo, Željko Reiner, Eric Bruckert, Claudia Stefanutti, Ioanna Gouni-Berthold, Colin Johnson, Alessia Di Costanzo, Elizabeth Hughes, Robert Dufour, Jan Borén, Xavier Pintó, Elizabeth Hughes, Alessia Di Costanzo, Jeanine Roeters Van Lennep, Jeanine Roeters Van Lennep, Handrean SoranChristophe Marçais, Erik Stroes, Xavier Pintó, Robert Cramb, Marcello Arca, Philippe Moulin, Luis Antonio Alvarez-Sala Walther

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2 Citazioni (Scopus)

Abstract

Data presented in this article are supplementary material to our article entitled “Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): expert panel recommendations 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 chylomicronaemia syndrome (MCS), from the validation and replication cohorts.
Lingua originaleEnglish
pagine (da-a)1334-1336
Numero di pagine3
RivistaData in Brief
Volume21
Stato di pubblicazionePublished - 2018

All Science Journal Classification (ASJC) codes

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