FOXP3 gene variations and susceptibility to autism: A case–control study

Autism Spectrum Disorders (ASD) are a group of heterogeneous neurodevelopmental disorders associated with immune system dysregulation. There are supporting evidences for the role of Forkhead Box P3 (FOXP3) gene as a lineage specification factor of regulatory T cells in the pathogenesis of ASD. The a...

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Veröffentlicht in:	Gene 2017-01, Vol.596, p.119-122
Hauptverfasser:	Safari, Mohammad Reza, Ghafouri-Fard, Soudeh, Noroozi, Rezvan, Sayad, Arezou, Omrani, Mir Davood, Komaki, Alireza, Eftekharian, Mohammad Mahdi, Taheri, Mohammad
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Autism Spectrum Disorders Autistic Disorder - genetics Case-Control Studies Child Female Forkhead Transcription Factors - genetics FOXP3 Genes, Dominant Genetic Predisposition to Disease Haplotypes Humans Immunity Iran Linkage Disequilibrium Male Polymorphism Polymorphism, Single Nucleotide
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