8. Interview with Melissa Bryce, Executive Director, The Global Foundation for Peroxisomal Disorders
We welcome Melissa Bryce, Executive Director, The Global Foundation for Peroxisomal Disorders. Join us to hear about these rare genetic disorders and how they impact the lives of many children and families. The Foundation's mission is to improve the lives of individuals with Peroxisomal Disorders by funding research, championing scientific collaboration and empowering families and professionals through educational support services.
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