Associated Papers
Heterogeneous nature of severe hypertriglyceridemia in childhood.
Ariza MJ et al.
Journal of Clinical Lipidology, 2026
The role of lipase maturation factor 1 in hypertriglyceridaemia and atherosclerosis: An update.
Dabravolski SA et al.
Sage Open Medicine, 2024
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
The Genetic Spectrum of Familial Hypertriglyceridemia in Oman.
Al-Waili K et al.
Frontiers in Genetics, 2022
Integrated Genomic, Functional, and Prognostic Characterization of Atypical Chronic Myeloid Leukemia.
Fontana D et al.
Hemasphere, 2020
33196013 (PubMed )
Supplement: hs9-4-e497-s009.xlsx › Sheet1
Genetic and functional studies of the LMF1 gene in Thai patients with severe hypertriglyceridemia.
Plengpanich W et al.
Molecular Genetics and Metabolism Reports, 2020
Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.
Takata A et al.
Nature Communications, 2019
31175295 (PubMed )
Supplement: 41467_2019_10482_MOESM8_ESM.xlsx › Supplementary_Data_5
Variants of Lipolysis-Related Genes in Korean Patients with Very High Triglycerides.
Lee CJ et al.
Yonsei Medical Journal, 2018
Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia.
Surendran RP et al.
Journal of Internal Medicine, 2012
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