Cargando…
Significant associations between 5-hydroxytryptaminetransporter-linked promoter region polymorphisms of the serotonin transporter (solute carrier family 6 member 4) gene and Thai patients with autism spectrum disorder
Autism spectrum disorder (ASD) is a form of pervasive developmental disorder manifested by impairment in social interactions and repetitive behaviors. Although genetic contribution is strongly suspected in autism, the specific genetic factors remain unidentified. Hyperserotoninemia has been reported...
Autores principales: | Wongpaiboonwattana, Wikrom, Plong-On, Oradawan, Hnoonual, Areerat, Limprasert, Pornprot |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478716/ https://www.ncbi.nlm.nih.gov/pubmed/32899028 http://dx.doi.org/10.1097/MD.0000000000021946 |
Ejemplares similares
-
Association between 19-bp Insertion/Deletion Polymorphism of Dopamine β-Hydroxylase and Autism Spectrum Disorder in Thai Patients
por: Wongpaiboonwattana, Wikrom, et al.
Publicado: (2022) -
Screening for FMR1 CGG Repeat Expansion in Thai Patients with Autism Spectrum Disorder
por: Hnoonual, Areerat, et al.
Publicado: (2021) -
Case Report: An Atypical Angelman Syndrome Case With Obesity and Fulfilled Autism Spectrum Disorder Identified by Microarray
por: Hnoonual, Areerat, et al.
Publicado: (2021) -
Whole-Exome Sequencing Identifies One De Novo Variant in the FGD6 Gene in a Thai Family with Autism Spectrum Disorder
por: Thongnak, Chuphong, et al.
Publicado: (2018) -
Novel Compound Heterozygous Mutations in the TRAPPC9 Gene in Two Siblings With Autism and Intellectual Disability
por: Hnoonual, Areerat, et al.
Publicado: (2019)