Clinical Trial Update: A Novel Mutation of the Spectrin Gene

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Summary

A completed clinical trial identified a novel mutation in the spectrin gene associated with hereditary elliptocytosis and hereditary pyropoikilocytosis.

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Diseases / indications

• Hereditary Elliptocytosis
• Hereditary Pyropoikilocytosis

Snippet

Sponsor: University of Utah | Conditions: Hereditary Elliptocytosis (HE), Hereditary Pyropoikilocytosis (HPP) | Status: COMPLETED