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Synaptic, transcriptional and chromatin genes disrupted in autism Associated with Submicroscopic 21q22 Deletion Including DYRK1A

October 30, 2014 DYRK1A

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In DYRK1A Gene Research Tags 2014 and older
← Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID. Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing →

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