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Clinical trial

Case Report: A Novel Mutation of the Spectrin Gene in a Family of Northern European Descent Is Associated With Three Different Phenotypes

NCT00723567 is registered in ClinicalTrials.gov with University of Utah as lead sponsor.

NCT NCT00723567
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Registry record

As filed in ClinicalTrials.gov.

Title
Case Report: A Novel Mutation of the Spectrin Gene in a Family of Northern European Descent Is Associated With Three Different Phenotypes
Lead sponsor
University of Utah
Phase
Observational
Overall status
Completed
Start date
February 29, 2008
Completion date
December 31, 2008
Enrollment
12 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

hereditary elliptocytosis (he), hereditary pyropoikilocytosis (hpp)