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FOXG1 Research Foundation
About
What is FOXG1 Syndrome?
Our Story
Our Mission
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Our Partners
Australia Chapter
We Remember
Contact Us
News / Blog
Research
Research & Development
Scientific Advisory Board
Path to a Cure
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FOXG1 Key Papers
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Ciitizen Natural History Study
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What is FOXG1 Syndrome?
Our Story
Our Mission
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Our Partners
Australia Chapter
We Remember
Contact Us
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Folder: Research
Back
Research & Development
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FOXG1 Key Papers
Folder: Parents & Caregivers
Back
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Blog Post Nicole Johnson 9/16/20 Blog Post Nicole Johnson 9/16/20

Un récapitulatif du Symposium scientifique FOXG1 2020

French translation of the recap of the FOXG1 Science Symposium 2020. Un récapitulatif du Symposium scientifique FOXG1 2020



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For two UB scientists, love means studying their daughter's rare disease
News Nicole Johnson 5/6/20 News Nicole Johnson 5/6/20

For two UB scientists, love means studying their daughter's rare disease

University at Buffalo biologists Soo-Kyung Lee (left) and Jae Lee are researching the FOXG1 gene. Their daughter, Yuna, has a mutation in the gene, which has severely impacted her development. The Lees hope their scientific work will lead to a treatment. Credit: Douglas Levere / University at Buffalo.

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