Associated Papers
Functional characterization of two DYRK1B variants causative of AOMS3.
Detro-Dassen S et al.
Orphanet Journal of Rare Diseases, 2024
DYRK1B haploinsufficiency in a family with metabolic syndrome and abnormal cognition.
Orenstein N et al.
Clinical Genetics, 2022
Two novel variants in DYRK1B causative of AOMS3: expanding the clinical spectrum.
Mendoza-Caamal EC et al.
Orphanet Journal of Rare Diseases, 2021
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