UnravelingRare A podcast produced by Unravel Biosciences to highlight patients, families, and other stakeholders critical to addressing orphan disorders. Episode 12:Forming a rare disease foundation - KMT2B Dystonia Foundation Episode 11:Meeting Rare Disease Stakeholders at the World Orphan Drug Congress Episode 10:Exponentially scaling drug discovery with COMBINED Brain Episode 09:Changing the drug discovery paradigm Episode 08:Exciting Progress at the CHOPS Foundation Symposium Episode 07:SPATA5L1 and the SPATA Foundation Episode 06:SPATA Disorder Episode 05:Story of successful repurposing for KMT2B syndrome Episode 04:CHOPS Syndrome and Synergies in Drug Development Episode 03:AP-4 Hereditary Spastic Paraplegia: solving multiple disorders at once Episode 13:Clinical success in Malan Syndrome Episode 02:Boys with Rett Syndrome Episode 01:Rett Syndrome in Latin America
