Associated Papers
The p.L218P variant in WDR83 disrupts neuronal development, leading to neurodevelopmental disorder.
Tabata H et al.
Scientific Reports, 2025
Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.
Kim DS et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2017
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