Ontology highlight
ABSTRACT:
SUBMITTER: Takumi T
PROVIDER: S-EPMC3261275 | biostudies-other | 2011 Sep
REPOSITORIES: biostudies-other
Journal of neurodevelopmental disorders 20110726 3
Autism is a neurodevelopmental disorder that manifests in childhood as social behavioral abnormalities, such as abnormal social interaction, impaired communication, and restricted interest or behavior. Of the known causes of autism, duplication of human chromosome 15q11-q13 is the most frequently associated cytogenetic abnormality. Chromosome 15q11-q13 is also known to include imprinting genes. In terms of neuroscience, it contains interesting genes such as Necdin, Ube3a, and a cluster of GABA(A ...[more]