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American Journal of Human Genetics|April 9, 2016
Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in InfancyChristine P Diggle, Stacey J Sukoff Rizzo, Michael Popiolek, et al.Nature|January 18, 2023
FinnGen provides genetic insights from a well-phenotyped isolated populationMitja I Kurki, Juha Karjalainen, Priit Palta, et al.Pageof 6