Association analysis of two synapse-related gene mutations with autism spectrum disorder in a Chinese population

Hou Fang; Li Li; Gong Jianhua; Chen Yanlin; Wang Jia; Liu Lingfei; Luo Xiu; Gu HuaiTing; Zhang Jiajia; Song Ranran

首页> 外文期刊>Research in autism spectrum disorders >Association analysis of two synapse-related gene mutations with autism spectrum disorder in a Chinese population

【24h】

Association analysis of two synapse-related gene mutations with autism spectrum disorder in a Chinese population

机译：中国人口中自闭症谱系紊乱的两个突触相关基因突变的关联分析

获取原文

获取原文并翻译 | 示例

掌桥外文数据库（机构版） >>

开具论文收录证明 >>

文献代查 >>

页面导航

摘要
著录项
相似文献
相关主题

摘要

Background: Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with a Keywords: strong genetic basis. Recently, synaptic abnormality has been proved to have a strong association Polymorphism with the etiology of ASD. PSD95 and DLGAP2 are the members of postsynaptic scaffolding PSD95 proteins that play crucial roles in synaptic plasticity and function. This study evaluated the association of the genetic variants in PSD95 and DLGAP2 with ASD. Autism spectrum disorder

机译：背景：自闭症谱系障碍（ASD）是一种复杂的神经开发障碍，具有关键词：强遗传基础。最近，已经证明突触异常具有强烈的关联多态性与ASD的病因。 PSD95和DLGAP2是突触后脚手架PSD95蛋白的成员，其在突触可塑性和功能中起重要作用。该研究评估了与ASD的PSD95和DLGAP2中的遗传变异的关联。自闭症谱系障碍

著录项

来源
《Research in autism spectrum disorders》 |2018年第2018期|共6页
作者
Hou Fang; Li Li; Gong Jianhua; Chen Yanlin; Wang Jia; Liu Lingfei; Luo Xiu; Gu HuaiTing; Zhang Jiajia; Song Ranran;
展开▼
作者单位

Huazhong Univ Sci &

Technol Tongji Med Coll Sch Publ Hlth Dept Maternal &

Child Hlth 13;

Matern &

Children Hlth Care Hosp Luohu Dist Shenzhen 518019 Peoples R China;

Matern &

Children Hlth Care Hosp Luohu Dist Shenzhen 518019 Peoples R China;

Matern &

Children Hlth Care Hosp Luohu Dist Shenzhen 518019 Peoples R China;

Huazhong Univ Sci &

Technol Tongji Med Coll Sch Publ Hlth Dept Maternal &

Child Hlth 13;

Huazhong Univ Sci &

Technol Tongji Med Coll Sch Publ Hlth Dept Maternal &

Child Hlth 13;

Huazhong Univ Sci &

Technol Tongji Med Coll Sch Publ Hlth Dept Maternal &

Child Hlth 13;

Huazhong Univ Sci &

Technol Tongji Med Coll Sch Publ Hlth Dept Maternal &

Child Hlth 13;

Univ South Carolina Arnold Sch Publ Hlth Dept Epidemiol &

Biostat Columbia SC 29208 USA;

Huazhong Univ Sci &

Technol Tongji Med Coll Sch Publ Hlth Dept Maternal &

Child Hlth 13;

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类神经病学与精神病学;
关键词
Polymorphism; PSD95; DLGAP2; Autism spectrum disorder;

机译：多态性;PSD95;DLGAP2;自闭症谱系障碍;

相似文献

外文文献
中文文献
专利

1. Association analysis of two synapse-related gene mutations with autism spectrum disorder in a Chinese population [J] . Hou Fang, Li Li, Gong Jianhua, Research in autism spectrum disorders . 2018,第期

机译：中国人口中自闭症谱系紊乱的两个突触相关基因突变的关联分析
2. Analysis of serotonin receptor 2A gene (HTR2A): association study with autism spectrum disorder in the Indian population and investigation of the gene expression in peripheral blood leukocytes. [J] . Guhathakurta S, Singh AS, Sinha S, Neurochemistry International: The International Journal for the Rapid Publication of Critical Reviews, Preliminary and Original Research Communications in Neurochemistry . 2009,第8期

机译：血清素受体2A基因（HTR2A）分析：与印度人自闭症谱系障碍的关联研究以及外周血白细胞基因表达的调查。
3. Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population. [J] . Dutta S, Sinha S, Ghosh S, Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences . 2008,第1期

机译：reelin基因（RELN）SNP的遗传分析：在印度人口中与自闭症谱系障碍无关联。
4. Analysis of GABRB1 association with Autism in Chinese Han Population with SNP genotyping [C] . Yuanzhuo Zheng, Yu Sun, Wenjing Chen, International Forum on Progress on Post-Genome Technologies(5'IFPT); 20070910-11; Suzhou(CN) . 2007

机译：SNP基因分型对中国汉族人群GABRB1与自闭症的关联分析
5. Talking with bilingual Chinese-American immigrant parents of children with autism spectrum disorders about intergenerational language practices. [D] . Yu, Betty. 2009

机译：与自闭症谱系障碍儿童的双语华裔移民父母讨论代际语言习俗。
6. Association Study of Polymorphisms in Genes Relevant to Vitamin B12 and Folate Metabolism with Childhood Autism Spectrum Disorder in a Han Chinese Population [O] . Zengyu Zhang, Lianfang Yu, Sufang Li, 1923

机译：汉族人群维生素B12和叶酸代谢相关基因多态性与儿童自闭症谱系的关联研究
7. Association Study of Polymorphisms in Genes Relevant to Vitamin B12 and Folate Metabolism with Childhood Autism Spectrum Disorder in a Han Chinese Population [O] . Zengyu Zhang, Lianfang Yu, Sufang Li, 2018

机译：汉族人口中儿童自闭症谱系与幼儿自闭症谱系相关基因多态性研究

Association analysis of two synapse-related gene mutations with autism spectrum disorder in a Chinese population

摘要

著录项

相似文献

相关主题

期刊订阅