Involvement of tryptophan hydroxylase 2 gene polymorphisms in susceptibility to tic disorder in Chinese Han population.
第一作者:
Ping,Zheng
第一单位:
Department of Neurological medicine, Capital Institute of Pediatrics, Beijing, 100020, China.
作者:
主题词
发病年龄(Age of Onset);等位基因(Alleles);动物(Animals);注意力缺陷障碍伴多动(Attention Deficit Disorder with Hyperactivity);结合部位(Binding Sites);病例对照研究(Case-Control Studies);儿童(Child);中国(China);DNA(DNA);数据说明, 统计(Data Interpretation, Statistical);女(雌)性(Female);基因频率(Gene Frequency);基因型(Genotype);单倍型(Haplotypes);人类(Humans);连锁不平衡(Linkage Disequilibrium);男(雄)性(Male);神经心理学测验(Neuropsychological Tests);多态现象, 遗传(Polymorphism, Genetic);多态性, 单核苷酸(Polymorphism, Single Nucleotide);性别因素(Sex Factors);抽搐性运动障碍(Tic Disorders);转录因子(Transcription Factors);色氨酸羟化酶(Tryptophan Hydroxylase)
DOI
10.1186/1744-9081-9-6
PMID
23360517
发布时间
2022-12-07
- 浏览2
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文