Генетические дефекты при аутизме: K. Wang, H. Zhang, D. Ma, et al., Common Genetic Variants on 5p14.1 Associate with Autism Spectrum Disorders, Nature 459 (2009): 528–533; R. Moessner, C. R. Marshall, J. S. Sutcliffe, et al., Contribution of SHANK-3 Mutations to Autism Spectrum Disorder, American Journal of Human Genetics 81 (2007): 1289–1297; K. Garber, Autism’s Cause May Reside in Abnormalities of the Synapse, Science 317 (2007): 190–191; L. A. Weiss, Y. Shen, J. M. Korn, et al., Association Between Microdeletion and Microduplication at 16p11.2 and Autism, New England Journal of Medicine 358 (2008): 667–675.
