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No Evidence for Association Between Norepinephrine Transporter-3081 (A/T) Polymorphism and Attention Deficit Hyperactivity Disorder in Iranian Population

机译：没有证据表明伊朗人群中去甲肾上腺素转运蛋白-3081（A / T）多态性与注意力缺陷多动障碍之间没有关联

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Background:Attention Deficit Hyperactivity Disorder (ADHD) can lead to drastic problems for the patient and its worldwide prevalence is 5%-12%. It also has many comorbidities with other disorders, and the genetic contribution seems the most significant cause.

机译：背景：注意力缺陷多动障碍（ADHD）可能导致患者出现严重问题，其全球患病率为5％-12％。它也与其他疾病并存许多疾病，遗传因素似乎是最重要的原因。

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期刊名称 Iranian Red Crescent Medical Journal
作者
Mohammad Reza Eslami Amirabadi; Rozita Davari-Ashtiani; Mojgan Khademi; Sepideh RajeziEsfahani; Babak Emamalizadeh; Abolfazl Movafagh; Fariba Arabgol; Said Sadr; Hossein Darvish; Katayoon Razjouyan;
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作者单位

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年(卷),期 2015(17),7
年度 2015
页码 e22996
总页数 5
原文格式 PDF
正文语种
中图分类
关键词
SCL6A2 Protein Humans Attention Deficit Disorder with Hyperactivity Polymorphism Genetic Iran;

机译：SCL6A2蛋白;人类;注意力缺陷多动障碍;多态性;遗传;伊朗;

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专利

1. No Evidence for Association Between Norepinephrine Transporter-3081 (A/T) Polymorphism and Attention Deficit Hyperactivity Disorder in Iranian Population [J] . Mohammad Reza Eslami Amirabadi 1, Rozita Davari-Ashtiani 3, Mojgan Khademi 3, Iranian red crescent medical journal . 2015,第7期

机译：没有证据表明伊朗人群中去甲肾上腺素转运蛋白-3081（A / T）多态性与注意缺陷多动障碍之间没有关联
2. No evidence of an association between norepinephrine transporter gene polymorphisms and attention deficit hyperactivity disorder. A family-based and case-control association study in a Korean sample. [J] . Cho SC, Kim JW, Kim BN, Neuropsychobiology . 2008,第3期

机译：没有证据表明去甲肾上腺素转运蛋白基因多态性与注意力缺陷多动障碍有关。在韩国样本中进行的基于家庭和病例对照协会的研究。
3. No evidence of an association between norepinephrine transporter gene polymorphisms and attention deficit hyperactivity disorder. A family-based and case-control association study in a Korean sample. [J] . Cho SC, Kim JW, Kim BN, Neuropsychobiology . 2008,第3期

机译：没有证据表明去甲肾上腺素转运蛋白基因多态性与注意力缺陷多动障碍有关。在韩国样本中进行的基于家庭和病例对照协会的研究。
4. Urinary Inorganic Arsenic Concentration and Attention Deficit-Hyperactivity Disorder: A Population-Based Analysis in Arica, Chile [C] . Maria P. Munoz, Paola A. Rubilar, Macarena Valdes, Joint annual meeting of the International Society of Exposure Science and the International Society for Environmental Epidemiology . 2018

机译：尿无机砷浓度和注意缺陷多动障碍：智利阿里卡的基于人口的分析
5. Attention Deficit Hyperactivity Disorder (ADHD) in adolescents: An investigative study of dopamine NAD norepinephrine systems. [D] . Knight, Katherine Ellis. 2013

机译：青少年注意力缺陷多动障碍（ADHD）：多巴胺和去甲肾上腺素系统的一项调查研究。
6. Association analysis of DISC1 gene polymorphisms with Attention-Deficit Hyperactivity Disorder in Iranian population [O] . Matin Kayyal, Abolfazl Movafagh, Mehrdad Hashemi, 2015

机译：伊朗人群DISC1基因多态性与注意力缺陷多动障碍的关联分析
7. Association studies of -3081(A/T) polymorphism of norepinephrine transporter gene with attention deficit/hyperactivity disorder in Korean population. [O] . Joung Y, Kim CH, Moon J, 2011

机译：去甲肾上腺素转运蛋白基因-3081（A / T）多态性与韩国人群注意缺陷/多动障碍的相关性研究。

No Evidence for Association Between Norepinephrine Transporter-3081 (A/T) Polymorphism and Attention Deficit Hyperactivity Disorder in Iranian Population

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