An investigation of ribosomal protein L10 gene in autism spectrum disorders

• Main Authors: Rastam Maria (Author), Anckarsäter Henrik (Author), Nygren Gudrun (Author), Goubran-Botros Hany (Author), Betancur Catalina (Author), Chaste Pauline (Author), Durand Christelle M (Author), Fauchereau Fabien (Author), Delorme Richard (Author), Gong Xiaohong (Author), Gillberg I Carina (Author), Kopp Svenny (Author), Mouren-Simeoni (Author), Gillberg Christopher (Author), Leboyer Marion (Author), Bourgeron Thomas (Author)
• Format: Book
• Published: BMC, 2009-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Autism spectrum disorders (ASD) are severe neurodevelopmental disorders with the male:female ratio of 4:1, implying the contribution of X chromosome genetic factors to the susceptibility of ASD. The ribosomal protein L10 (RPL10) gene...