AI Networking Cookbook: Practical recipes for AI-assisted network automation and development
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Chiari I Malformation as a Human Disease Model of Cerebellar Cognitive–Affective Dysfunction
De novo chromatin remodelling variants in sporadic Chiari 1 malformation.
Chiari 1 malformation (CM1) is the most common congenital malformation of the human hindbrain. Although prior studies have implicated chromatin-remodeling genes in CM1, the de novo genetic architecture and underlying neurodevelopmental mechanisms remain incompletely defined. To investigate the molecular genetics of a n...