Study
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?
