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Genetics in Medicine Open
(Jan 2024)
P171: Developing an approach to screening rare genetic diagnoses for amenability to bespoke genetic therapy development
David Cheerie,
Marlen Lauffer,
Danique Beijer,
Matthis Synofzik,
Annemieke Aartsma-Rus,
Michael Szego,
Kimberly Amburgey,
Brian Kalish,
James Dowling,
Gregory Costain
Affiliations
David Cheerie
Genetics and Genome Biology, SickKids Research Institute, Toronto, ON, Canada
Marlen Lauffer
Dutch Center for RNA Therapeutics, Leiden University Medical Center, The Netherlands
Danique Beijer
Hertie-Institute for Clinical Brain Research, University of Tübingen, Germany
Matthis Synofzik
Hertie-Institute for Clinical Brain Research, University of Tübingen, Germany
Annemieke Aartsma-Rus
Dutch Center for RNA Therapeutics, Leiden University Medical Center, The Netherlands
Michael Szego
Joint Centre for Bioethics, University of Toronto, Toronto, ON, Canada
Kimberly Amburgey
Genetics and Genome Biology, SickKids Research Institute, Toronto, ON, Canada
Brian Kalish
Neurosciences and Mental Health, SickKids Research Institute, Toronto, ON, Canada
James Dowling
Genetics and Genome Biology, SickKids Research Institute, Toronto, ON, Canada
Gregory Costain
Genetics and Genome Biology, SickKids Research Institute, Toronto, ON, Canada
Journal volume & issue
Vol. 2
p. 101068
Abstract
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No abstracts available.
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