MECP2 and autism

Kim, S-J. and Cook, E.H.: Novel de novo nonsense mutation of MECP2 in a patient with Rett syndrome. Human Mutation 2000,15:382-383

Beyer, K.S., Blasi, F., Bacchelli, E., Klauck, S.M., Maestrini, E., Poustka, A., International Molecular Genetic Study of Autism Consortium (IMGSAC): Mutation analysis of the coding sequence of the MECP2 gene in infantile autism. Human Genetics 2002,111:305-309

Zappella, M. et al. Study of MECP2 gene in Rett syndrome variants and autistic girls. American Journal of Medical Genetics (Neuropsychiatric Genetics) 2003,116B:online

Laboratory of Developmental Neuroscience Home Page