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.

Additional Metadata
Persistent URL dx.doi.org/10.1016/j.dib.2018.10.125, hdl.handle.net/1765/112034
Journal Data in Brief
Citation
Moulin, P. (Philippe), Dufour, R. (Robert), Averna, M, Arca, M, Cefalù, A.B, Noto, D. (Davide), … Bruckert, E. (2018). Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score. Data in Brief, 21, 1334–1336. doi:10.1016/j.dib.2018.10.125