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Functional characterization of DYRK1A missense variants associated with a syndromic form of intellectual deficiency and autism

April 15, 2018 Amy Clugston

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In DYRK1A Gene Research Tags Present Day - 2015
← A comprehensive proteomics-based interaction screen that links DYRK1A to RNF169 and to the DNA damage responseClinical phenotype of ASD-associated DYRK1A haploinsufficiency →

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