Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

Pokaż inne wersje (1)

Background: Autism spectrum disorder (ASD) is characterised by impairments in social communication and by a pattern of repetitive behaviours, with learning disability (LD) typically seen in up to 70% of cases. A recent study using the PPL statistical framework identified a novel region of genetic li...

Szczegółowa specyfikacja

Opis bibliograficzny
Główni autorzy: Pagnamenta, A, Khan, H, Walker, S, Gerrelli, D, Wing, K, Bonaglia, M, Giorda, R, Berney, T, Mani, E, Molteni, M, Pinto, D, Le Couteur, A, Hallmayer, J, Sutcliffe, J, Szatmari, P, Paterson, A, Scherer, S, Vieland, V, Monaco, A
Format: Journal article
Język:English
Wydane: 2011

Podobne zapisy