Rett Syndrome Without MECP2: Single Gene Variant Rewrites the Diagnostic Story
Swedish researchers report that a de novo variant in the GABBR2 gene, which encodes a GABA-B receptor subunit, caused classic ...
Swedish researchers report that a de novo variant in the GABBR2 gene, which encodes a GABA-B receptor subunit, caused classic ...
A network meta-analysis of 25 randomized controlled trials finds that functional training combined with sensory rehabilitation programs ranks highest for ...
New research indicates that pathogenic variants in the NLGN4X gene disrupt both synaptic connectivity and cortical development, offering a broader ...
A meta-analysis of 309 randomized controlled trials finds that physical activity interventions for neurodevelopmental disorders do not significantly increase adverse ...
A large clinic-based study of over 1,400 children with fragile X syndrome maps the frequency, severity, and co-occurrence of the ...
© 2025 Scienmag - Science Magazine
© 2025 Scienmag - Science Magazine