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DYRK1A mutations in two unrelated patients

March 1, 2015 DYRK1A

Read Abstract

In DYRK1A Gene Research, DYRK1A Patient Research Tags Present Day - 2015
← Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID. →

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