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

Research output: Contribution to journalArticlepeer-review

2 Citations (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.
Original languageEnglish
Pages (from-to)1334-1336
Number of pages3
JournalData in Brief
Volume21
Publication statusPublished - 2018

All Science Journal Classification (ASJC) codes

  • General

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