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linkedin.com
#facesofgenetherapy | Institute for Gene Therapies
IGT is helping to raise the volume on rare disease awareness throughout the month of February. In a recent conversation with Foundation for Angelman Syndrome Therapeutics (FAST)'s Allyson Berent, IGT Chair Erik Paulsen covered the unfortunate reality that many genetic conditions share the same barriers: slow translation, limited funding, and ...
1 month ago
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Angelman syndrome is a rare disorder that affects chromosome 15, resulting in intellectual and developmental delay. Common signs and symptoms usually appear in early childhood but despite these symptoms, people with Angelman syndrome have an overall happy and excitable demeanor. #InternationalAngelmanDay #angelmanday2024 | Angelman Syndrome Foundation
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