Discovering a rare genetic disorder: Extended interview with Scott Bell
Sep 21, 2019•15 min
Episode description
Science Journalists Alyssia and Julianna ask Scott Bell some hard hitting questions regarding his research investigating rare genetic diseases in youth. Scott is a PhD student at McGill University based at the Douglas Mental Health University Institute. Using advanced genetic techniques including making neurons from stem cells, Scott recently led a ground breaking discovery identifying a new neurodevelopmental disease cause by mutation in a brain gene called ACTL6B.
You can read more about Scott's work here:
https://www.mcgill.ca/newsroom/channels/news/quebec-siblings-rare-orphan-disease-lead-discovery-rare-genetic-diseases-296454
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