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
Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score / Moulin, P; Dufour, R; Averna, M; Arca, M; Cefalù, Ab; Noto, D; D'Erasmo, L; Di Costanzo, A; Marçais, C; Walther, Laa; Banach, M; Borén, J; Cramb, R; Gouni-Berthold, I; Hughes, E; Johnson, C; Pintó, X; Reiner, Ž; van Lennep, Jr; Soran, H; Stefanutti, C; Stroes, E; Bruckert, E. - In: DATA IN BRIEF. - ISSN 2352-3409. - 21:(2018), pp. 1334-1336. [10.1016/j.dib.2018.10.125]
Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score
Arca MMembro del Collaboration Group
;D'Erasmo L;Di Costanzo A;Hughes E;Stefanutti C;
2018
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| File | Dimensione | Formato | |
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Moulin_patients-FCS_2018.pdf
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