Associated Papers
Biochemical, Clinical, and Genetic Characteristics of Mexican Patients with Primary Hypertriglyceridemia, Including the First Case of Hyperchylomicronemia Syndrome Due to GPIHBP1 Deficiency.
Rodríguez-Gutiérrez PG et al.
International Journal of Molecular Sciences, 2022
Genetic variants in triglyceride metabolism genes among individuals with hypertriglyceridemia in Colombia.
Puerto-Baracaldo K et al.
Journal of Clinical Lipidology, 0
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