Autism is a hard disorder to nail down genetically- single nucleotide polymorphisms (SNPs) or even multiple locus genetic effects are not able to account for the large genetic component to the disorder. In recent times, Copy number variations (CNVs) has come to the forefront of Autism research , suggesting that microdeletions, duplications etc [...]Rating: 0.0/10 (0 votes cast)
Related posts:CNVs and Autism/ Schizophrenia I had been meaning to comment on a recent paper...Autism, Schizophrenia and CNV in 16p11.2 Image via Wikipedia There is a letter published in...The Default Brain Network: implications for Autism and Schizophrenia This blog post has been triggered by a recent news......
Gregory, S., Connelly, J., Towers, A., Johnson, J., Biscocho, D., Markunas, C., Lintas, C., Abramson, R., Wright, H., Ellis, P.... (2009) Genomic and epigenetic evidence for oxytocin receptor deficiency in autism. BMC Medicine, 7(1), 62. DOI: 10.1186/1741-7015-7-62 Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
Gurrieri, F., & Neri, G. (2009) Defective oxytocin function: a clue to understanding the cause of autism?. BMC Medicine, 7(1), 63. DOI: 10.1186/1741-7015-7-63 Defective oxytocin function: a clue to understanding the cause of autism?
Comments