Kate Mowery
Complex Commercial and IP Litigator | Rare Disease Advocate (FOXP1 Syndrome)
- Role
- Co-founder, Vice President at International Foxp1 Foundation
- Location
- Wilmington, DE, US
- LinkedIn followers
- 500 followers
Experience
Co-founder, Vice President
International Foxp1 Foundation
Oct 2020 — Present
FOXP1 Syndrome is rare genetic syndrome defined by a deletion of or mutation on the FOXP1 gene and frequently presents with characteristics of low muscle tone, impaired verbal skills, and global developmental delays. Working with other parents of children with FOXP1 Syndrome, I helped co-found the International FOXP1 Foundation. Together, we work on behalf of all FOXP1 families with doctors, scientists, and medical organizations to advance the knowledge and resources for families and individuals with FOXP1 Syndrome.
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