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Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID.

February 24, 2015 DYRK1A

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In DYRK1A Gene Research, DYRK1A Patient Research Tags Present Day - 2015
← DYRK1A mutations in two unrelated patients Synaptic, transcriptional and chromatin genes disrupted in autism Associated with Submicroscopic 21q22 Deletion Including DYRK1A →

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