Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score
- Autori: Moulin, Philippe; Dufour, Robert; Averna, Maurizio; Arca, Marcello; Cefalù, Angelo B.; Noto, Davide; D'Erasmo, Laura; Di Costanzo, Alessia; Marçais, Christophe; Walther, Luis Antonio Alvarez-Sala; Banach, Maciej; Borén, Jan; Cramb, Robert; Gouni-Berthold, Ioanna; Hughes, Elizabeth; Johnson, Colin; Pintó, Xavier; Reiner, Željko; van Lennep, Jeanine Roeters; Soran, Handrean; Stefanutti, Claudia; Stroes, Erik; Bruckert, Eric*
- Anno di pubblicazione: 2018
- Tipologia: Articolo in rivista (Articolo in rivista)
- OA Link: http://hdl.handle.net/10447/332944
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.