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How has our understanding of Fragile X syndrome changed over the last 20 years? Dr. Mark Bear, Picower Professor of Neuroscience at MIT and FRAXA Investigator, joined the Fragile X field in 1999 when he received a research grant from FRAXA Research Foundation. At the time, we recognized the symptoms of Fragile X, and we knew its cause: a single missing protein. But we knew very little else. Dr. Bear traces the discoveries that now give us great optimism of finding effective treatments and ultimately a cure for Fragile X. Watch the entire Fragile X Syndrome: In Pursuit of a Cure Webinar https://www.fraxa.org/fragile-x-syndr... FRAXA’s mission is to find effective treatments and ultimately a cure for Fragile X syndrome. We directly fund research grants and fellowships at top universities around the world. We partner with biomedical and pharmaceutical companies, large and small, to bridge the gap between research discoveries and actual treatments. Treatments for Fragile X are likely to help people affected by autism, Alzheimer’s, and other brain disorders. To learn more about FRAXA's Fragile X syndrome research, to get involved with Fragile X awareness and events or to donate to FRAXA research, visit www.fraxa.org Let's Connect Facebook: / fraxaresearch Instagram: / fraxaresearch LinkedIn: / fraxa-research-foundation Twitter: / fraxaresearch Website: https://www.fraxa.org