Last Updated: 09/26/2026
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Found 2 publications
Novel Causative Variants in DYRK1A, KARS, and KAT6A Associated with Intellectual Disability and Additional Phenotypic Features.
Journal: Journal of pediatric genetics
Published: September 26, 2016
Mutations in TBCK, Encoding TBC1-Domain-Containing Kinase, Lead to a Recognizable Syndrome of Intellectual Disability and Hypotonia.
Journal: American journal of human genetics
Published: November 29, 2015
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Last Updated: 09/26/2026