Serotonin transporter gene promoter polymorphism and autism: A family-based genetic association study in Japanese population

التفاصيل البيبلوغرافية
العنوان: Serotonin transporter gene promoter polymorphism and autism: A family-based genetic association study in Japanese population
المؤلفون: Hideo Matsumoto, Kenji Yamamoto, Mariko Atsumi, Eiji Nanba, Youichi Enseki, Akitoshi Oya, Nobumasa Kato, Arata Asakura, Tomiei Iga, Shinko Koishi, Kosuke Yamazaki, Yutaka Aoki, Jyoji Inomata, Tetsuo Ishii, Tsukasa Sasaki, Seiji Koishi, Hidetoshi Inoko
المصدر: Brain and Development. 28:257-260
بيانات النشر: Elsevier BV, 2006.
سنة النشر: 2006
مصطلحات موضوعية: Adult, Male, Serotonin, Linkage disequilibrium, Adolescent, DNA Mutational Analysis, Locus (genetics), Biology, Japan, Developmental Neuroscience, mental disorders, medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, Autistic Disorder, Promoter Regions, Genetic, Serotonin transporter, Genetic association, Brain Chemistry, Serotonin Plasma Membrane Transport Proteins, Genetics, Polymorphism, Genetic, Haplotype, Brain, Promoter, General Medicine, Transmission disequilibrium test, Middle Aged, medicine.disease, Mutation, Pediatrics, Perinatology and Child Health, biology.protein, Autism, Female, Neurology (clinical)
الوصف: Autism is now widely accepted as a biological disorder which, by and large, starts before birth. It has been shown that serotonin (5-HT) is associated with several psychological processes and hyperserotoninemia is observed in some autistic patients. The results of previous reports about family-based association studies between the serotonin transporter (5-HTT) gene promoter polymorphism and autism are controversial. In this study, an analysis using the transmission/disequilibrium test (TDT) between the 5-HTT gene promoter polymorphism and autism in 104 trios, all ethnically Japanese, showed no significant linkage disequilibrium (P=0.17). Recently, it has been reported that some haplotypes at the serotonin transporter locus may be associated with the pathogenesis of autism. Therefore, further investigations by haplotype analyses are necessary to confirm the implications of genetic variants of the serotonin transporter in the etiology of autism.
تدمد: 0387-7604
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78484a415ea153fa5527fd40aa69346a
https://doi.org/10.1016/j.braindev.2005.09.003
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....78484a415ea153fa5527fd40aa69346a
قاعدة البيانات: OpenAIRE