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Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature

February 27, 2016 DYRK1A

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In DYRK1A Gene Research, DYRK1A Patient Research Tags Present Day - 2015
← The GBA, DYRK1A and MS4A6A polymorphisms influence the age at onset of Chinese Parkinson patients. Characterizing autism spectrum disorders by key biochemical pathways →

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