A Novel Mutation of the Spectrin Gene
NCT00723567 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 12
Last updated 2009-02-19
Summary
The purpose of this study is to find a gene or its mutation (an altered gene) that puts individuals at risk for developing HE or HPP.
Conditions
- Hereditary Elliptocytosis (HE)
- Hereditary Pyropoikilocytosis (HPP)
Sponsors & Collaborators
-
University of Witwatersrand, South Africa
collaborator OTHER - lead OTHER
Principal Investigators
-
Josef T Prchal, MD · University of Utah
Eligibility
- Min Age
- 7 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2008-02-29
- Primary Completion
- 2008-12-31
- Completion
- 2008-12-31
Countries
- United States
Study Locations
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