eLife1d
Gene discovery sheds light on common ear condition in people with Down syndrome
The gene DYRK1A could be a potential therapeutic target to treat ‘glue ear’ in people with Down syndrome, according to a new study.
Genetic cause for main type of hearing loss in children with Down syndrome identified
The genetic cause for the most common type of hearing loss in children with Down syndrome has been identified in mice by ...
eLife1d
DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome
This study addresses fundamental questions surrounding otitis media effusion in Down syndrome, identifying DYRK1A as a key gene involved in the condition. The findings are compelling, highlighting ...