Evidence
Mol Neurobiol. 2023 Jun 6. doi: 10.1007/s12035-023-03405-9. Online ahead of print.
ABSTRACT
Autism spectrum disorder (ASD) is among the most widespread neurodevelopmental diseases, with an approximate prevalence rate of 1 in 59. From a genetic point of view, this disorder is highly heterogeneous. This disorder is associated with both inheritable and de novo mutations in several genes. In addition to genetic loci that are identified through early karyotype analyses, recent advent of high throughput sequencing methods has facilitated identification of several genetic loci that confer risk of ASD. The current review provides an overview of different types of identified mutations including missense and nonsense mutations and copy number variations in various genes in individuals affected with ASD.
PMID:37278883 | DOI:10.1007/s12035-023-03405-9
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