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cc-by (c) Moulin, Philippe et al., 2018
Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/184941

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

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Data presented in this article are supplementary material to our article entitled "Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): expert panel recom mendations 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 chylomicro naemia syndrome (MCS), from the validation and replication cohorts.

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MOULIN, Philippe, DUFOUR, Robert, AVERNA, Maurizio, ARCA, Marcello, CEFALÙ, Angelo b., NOTO, Davide, D'ERASMO, Laura, DI COSTANZO, Alessia, MARÇAIS, Christophe, ALVAREZ-SALA WALTHER, Luis antonio, BANACH, Maciej, BORÉN, Jan, CRAMB, Robert, GOUNI-BERTHOLD, Ionna, HUGHES, Elizabeth, JOHNSON, Colin, PINTÓ SALA, Xavier, REINER, Eljko, ROETERS VAN LENNEP, Jeanine, SORAN, Handrean, STEFANUTTI, Claudia, STROES, Erik, BRUCKERT, Eric. Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): establishment of an FCS clinical diagnostic score. _Data in Brief_. 2018. Vol. 21, núm. 1334-1336. [consulta: 25 de febrer de 2026]. ISSN: 2352-3409. [Disponible a: https://hdl.handle.net/2445/184941]

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