Treatment of Genetic Screening of Hypertriglyceridemia type I, III, and V - HTG Amsterdam
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This is a cohort of patients with extreme hypertriglyceridemia. Patients have been screened for loss of function mutations in LPL, GPIHBP1, APOC2, APOA5 and LMF1.]]> Inclusion:See Surendran RP et al., J Inte Med, 2012 TG >10 mmol/l Exclusion: ApoE2E2 Alcohol abuse Uncontrolled diabetes ]]> This is a cohort collected at the outpatient clinic of the AMC. Patients have been collected in the past 15 years.]]>
创建时间：
2012-10-02
