Clinical Trial Update: Analysis of Oculo-motor Deficiencies Associated With FMR1 Gene Expression (Genetic Abnormality Predisposing to a Neurodegenerative Disease) [NA]

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Summary

A clinical trial update notes the termination of a study investigating oculomotor deficits associated with FMR1 premutation, a genetic variation linked to Fragi…

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Diseases / indications

• Fragile X-associated Tremor Ataxia Syndrome

Snippet

Sponsor: Nantes University Hospital | Conditions: Pre-mutation on FMR1 Gene | NA | Status: TERMINATED