Genetics of autism: complex aetiology for a heterogeneous disorder

Since autism was first recognized as a disorder in 1943, speculation about its aetiology has ranged from biological to psychological and back again. After twin studies during the 1970s and 1980s yielded unequivocal evidence for a genetic component, aetiological research in autism began to focus prim...

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Veröffentlicht in:	Nature reviews. Genetics 2001-12, Vol.2 (12), p.943-955
Hauptverfasser:	Folstein, S E, Rosen-Sheidley, B
Format:	Artikel
Sprache:	eng
Schlagworte:	Autistic children Autistic Disorder - etiology Autistic Disorder - genetics Child & adolescent psychiatry chromosome 16 chromosome 2 chromosome 7 Chromosome Mapping DBH gene Etiology Eye contact Female FOXP2 gene GABRB3 gene Genetic Counseling Genetics Genome, Human Genomes GRIK2 gene Humans Male Neuropathology Parents & parenting Pathophysiology Phenotype RAY1 gene RELN gene Schizophrenia Social isolation SPCH1 gene Speech ST7 gene Twins UBE3A gene wnt2 gene
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