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We're fundraising for Hao-Fountain Syndrome Awareness!
What is Hao-Fountain Syndrome?
Hao-Fountain Syndrome is a neurodevelopmental disorder caused by a mutation of the USP7 gene. The USP7 gene is a protein-coding gene that plays a role in tumor suppression, transcriptional regulation, immune response, and endosomal protein recycling. Mutations are either point mutations or gene deletions. Currently, there are only 82 people world-wide with this diagnosis.
People diagnosed with Hao-Fountain Syndrome may have some of these symptoms:
Join me today in helping those diagnosed with Hao-Fountain Syndrome!
Make a donation to Team Name
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We're fundraising for Hao-Fountain Syndrome Awareness!
What is Hao-Fountain Syndrome?
Hao-Fountain Syndrome is a neurodevelopmental disorder caused by a mutation of the USP7 gene. The USP7 gene is a protein-coding gene that plays a role in tumor suppression, transcriptional regulation, immune response, and endosomal protein recycling. Mutations are either point mutations or gene deletions. Currently, there are only 82 people world-wide with this diagnosis.
People diagnosed with Hao-Fountain Syndrome may have some of these symptoms:
Join me today in helping those diagnosed with Hao-Fountain Syndrome!
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We're fundraising for Hao-Fountain Syndrome Awareness!
What is Hao-Fountain Syndrome?
Hao-Fountain Syndrome is a neurodevelopmental disorder caused by a mutation of the USP7 gene. The USP7 gene is a protein-coding gene that plays a role in tumor suppression, transcriptional regulation, immune response, and endosomal protein recycling. Mutations are either point mutations or gene deletions. Currently, there are only 82 people world-wide with this diagnosis.
People diagnosed with Hao-Fountain Syndrome may have some of these symptoms:
Join me today in helping those diagnosed with Hao-Fountain Syndrome!
Organization Name
Org Address Line 1
Org City, Org State Org Zip
Need help? Org Email