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FOXG1 Research Foundation
About
What is FOXG1 Syndrome?
Our Story
Our Mission
Our Team
Our Partners
Australia Chapter
We Remember
Contact Us
News / Blog
Research
Research & Development
Scientific Advisory Board
Path to a Cure
Research Assets & Grants
FOXG1 Key Papers
Parents & Caregivers
Newly Diagnosed
Resources
Ciitizen Natural History Study
Patient Data Center | Registry
Stem Cell Biobank
Brain Donation
Clinical Centers
Clinical Trial FAQ
FOXG1 Store
FUNDRAISING TEAMS
GET INVOLVED
Donate
Folder: About
Back
What is FOXG1 Syndrome?
Our Story
Our Mission
Our Team
Our Partners
Australia Chapter
We Remember
Contact Us
News / Blog
Folder: Research
Back
Research & Development
Scientific Advisory Board
Path to a Cure
Research Assets & Grants
FOXG1 Key Papers
Folder: Parents & Caregivers
Back
Newly Diagnosed
Resources
Ciitizen Natural History Study
Patient Data Center | Registry
Stem Cell Biobank
Brain Donation
Clinical Centers
Clinical Trial FAQ
FOXG1 Store
FUNDRAISING TEAMS
GET INVOLVED
Donate
FOXG1 Research Foundation's Nasha Fitter Speaks  At The White House Rare Disease Forum
News, YouTube, Announcement Nicole Johnson 3/4/24 News, YouTube, Announcement Nicole Johnson 3/4/24

FOXG1 Research Foundation's Nasha Fitter Speaks At The White House Rare Disease Forum

FOXG1 Research Foundation Co-founder and CEO Nasha Fitter was the first spotlight speaker at the White House Rare Disease Forum hosted by the White House Office of Science and Technology Policy's Health Outcomes Team February 28th ahead of Rare Disease Day 2024.

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