Cargando…
A Study of Single Nucleotide Polymorphisms of the SLC19A1/RFC1 Gene in Subjects with Autism Spectrum Disorder
Autism Spectrum Disorder (ASD) is a group of neurodevelopmental disorders with complex genetic etiology. Recent studies have indicated that children with ASD may have altered folate or methionine metabolism, suggesting that the folate–methionine cycle may play a key role in the etiology of ASD. SLC1...
Autores principales: | Mahmuda, Naila Al, Yokoyama, Shigeru, Huang, Jian-Jun, Liu, Li, Munesue, Toshio, Nakatani, Hideo, Hayashi, Kenshi, Yagi, Kunimasa, Yamagishi, Masakazu, Higashida, Haruhiro |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881591/ https://www.ncbi.nlm.nih.gov/pubmed/27213354 http://dx.doi.org/10.3390/ijms17050772 |
Ejemplares similares
-
Association Study between the CD157/BST1 Gene and Autism Spectrum Disorders in a Japanese Population
por: Yokoyama, Shigeru, et al.
Publicado: (2015) -
One Single Nucleotide Polymorphism of the TRPM2 Channel Gene Identified as a Risk Factor in Bipolar Disorder Associates With Autism Spectrum Disorder in a Japanese Population
por: Mahmuda, Naila Al, et al.
Publicado: (2020) -
Non-synonymous single-nucleotide variations of the human oxytocin receptor gene and autism spectrum disorders: a case–control study in a Japanese population and functional analysis
por: Ma, Wen-Jie, et al.
Publicado: (2013) -
Social Interaction Improved by Oxytocin in the Subclass of Autism with Comorbid Intellectual Disabilities
por: Higashida, Haruhiro, et al.
Publicado: (2019) -
Oxytocin for Male Subjects with Autism Spectrum Disorder and Comorbid Intellectual Disabilities: A Randomized Pilot Study
por: Munesue, Toshio, et al.
Publicado: (2016)