Genetic Study of Sitosterolemia
NCT00004481 · Status: COMPLETED · Type: OBSERVATIONAL
Last updated 2005-06-24
Summary
OBJECTIVES:
I. Identify the genetic defect and fine map the gene that causes sitosterolemia.
Conditions
- Lipid Metabolism, Inborn Errors
- Sitosterolemia
Interventions
- PROCEDURE
-
genetic testing
Sponsors & Collaborators
-
Medical University of South Carolina
collaborator OTHER -
National Center for Research Resources (NCRR)
lead NIH
Principal Investigators
-
Shailesh B. Patel · Medical University of South Carolina
Eligibility
- Min Age
- 0 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 1999-11-30
Countries
- United States
Study Locations
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