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The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy

October 25, 2012 DYRK1A

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In DYRK1A Gene Research, DYRK1A Patient Research Tags 2014 and older
← Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disord Dyrk1A, a serine/threonine kinase, is involved in ERK and Akt activation in the brain of hyperhomocysteinemic mice. →

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