Understanding copy number variations through their genes: a molecular view on 16p11.2 deletion and duplication syndromes

• Asıl Yazarlar: Roberta Leone (Yazar), Cecilia Zuglian (Yazar), Riccardo Brambilla (Yazar), Ilaria Morella (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Frontiers Media S.A., 2024-06-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

Neurodevelopmental disorders (NDDs) include a broad spectrum of pathological conditions that affect >4% of children worldwide, share common features and present a variegated genetic origin. They include clinically defined diseases, such as autism spectrum disorders (ASD), attention-deficit/hypera...