Treatment of genetic screening of hypertriglyceridemia type I, III, and V - HTG Amsterdam

Study ID Alternative Stable ID Type
phs000511 Probands

Study Description

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.

Archive Link Archive Accession
dbGaP phs000511

Who archives the data?

There are no publications available