Characterizing familial chylomicronemia syndrome: Baseline data of the APPROACH study

Autor: Linda C. Hemphill, Raul D. Santos, Dirk J. Blom, Seth J. Baum, Andres Digenio, Ewa Karwatowska-Prokopczuk, Joseph L. Witztum, Ovidio Muñiz-Grijalvo, Louis O'Dea, Karren R Williams, Veronica J. Alexander

Publikováno v: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

Background Familial chylomicronemia syndrome (FCS) is a rare metabolic disorder caused by mutations in lipoprotein lipase (LPL) or genes required for LPL functionality and is characterized by hyperchylomicronemia that results in recurrent episodes of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84e6c733609c82f480fc505ff6fa785f
https://pubmed.ncbi.nlm.nih.gov/30318066