Study Description

This is a cohort of patients with extreme hypertriglyceridemia. Patients have been screened for loss of function mutations in LPL,... Show More

Study Accession Alternative Stable ID type
phs000511.v1.p1 dbGaP Probands; Mendelian; Family

Who controls access to this study

National Human Genome Research Institute
Access information:

Publications

21597005
20657596
22239554

Data provider(s)

  • Title Name Institute
    Principal Investigator E.S.G.Stroes, Prof. Dr AMC, University of Amsterdam, Amsterdam, The Netherlands
    Principal Investigator G.M.Dallinga-Thie, PhD AMC, University of Amsterdam, Amsterdam, The Netherlands
    Co-Investigator Sekar Kathiresan, MD Massachusetts General Hospital, Boston, MA, USA
    Funding Source U54 HG003067 National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA

Who archives the data?

The database of Genotypes and Phenotypes (dbGaP)