Study for people with FOXP1 gene changes
Part of Brain & nervous system, Mental health clinical trials.
This study looks at how people with FOXP1-related neurodevelopmental conditions work and how they’re affected, using genetic, medical, and thinking/learning tests. It may help researchers better understand the condition and improve future care.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You must have a recorded genetic change (variant) in the FOXP1 gene that is likely or definitely harmful (pathogenic)
- You must be at least 2 years old
- Your FOXP1 genetic result must be something the study team agrees with as likely/definitely pathogenic
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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