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Article

Genetic basis of hypertriglyceridemia.

Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis - 1 Dec 2024

Ariza Corbo María José, Muñiz-Grijalvo Ovidio, Blanco Echevarría Agustín, Díaz-Díaz J L

Abstract excerpt

The development of massive sequencing techniques and guidelines for assessing the pathogenicity of variants are allowing us the identification of new cases of familial chylomicronemia syndrome (FCS) mostly in the LPL gene, less frequently in GPIHBP1 and APOA5, and with even fewer cases in LMF1 and APOC2. From the included studies, it can be deduced that, in cases with multifactorial chylomicronemia syndrome...

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PMID: 39672669
DOI: 10.1016/j.arteri.2024.11.001

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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