Clinical Trial Update: MYT1L Syndrome: a Rare Paediatric Genetic Syndrome Responsible for a Neurodevelopmental Disorder

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Summary

A clinical trial in Rouen is recruiting to study MYT1L Syndrome, a rare paediatric genetic neurodevelopmental disorder. The study is sponsored by University Hos…

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Diseases / indications

• Myt1l Syndrome

Snippet

Sponsor: University Hospital, Rouen | Conditions: MYT1L Syndrome | Status: RECRUITING