Genetic Study of Sitosterolemia

Completed

Conditions studied: Lipid Metabolism, Inborn Errors, Sitosterolemia

In brief

OBJECTIVES: I. Identify the genetic defect and fine map the gene that causes sitosterolemia.

Key facts

Study ID

NCT00004481

Run by

National Center for Research Resources (NCRR)

Starts

1999-11-01

Last updated by the study team

2005-06-24

Who can join

Age: any. Sex: any. Healthy volunteers: accepted.

Where it is running

• Medical University of South Carolina — Charleston, South Carolina, United States

Full record on ClinicalTrials.gov

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