位置：成果数据库 > 期刊 > 期刊详情页
Mutation screening of the HTR2B gene in patients with Tourette syndrome
  • ISSN号：0304-3940
  • 期刊名称：Neurosci Lett
  • 时间：2012
  • 页码：150-153
  • 相关项目：非综合征型屈曲指的遗传研究
作者： Joseph Jankovic|Linyan Su|Jianguo Zhang|Weidong Le|Hongbo Xu|Zhijian Yang|Junxiang Tang|Shoujin Kuang|Hao Deng|
同期刊论文项目
非综合征型屈曲指的遗传研究
期刊论文 29
同项目期刊论文
Genetic analysis of the ATP1B4 gene in Chinese Han patients with Parkinson's disease
Analysis of the MRPL3, DNAJC13 and OFCC1 variants in Chinese Han patients with TS-CTD
EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease
Genetic analysis of the F-box only protein 41 gene in Chinese Han patients with Parkinson's dis
Analysis of the BTBD9 and HTR2C variants in Chinese Han patients with Tourette syndrome
Genetic analysis of the fused in sarcoma gene in Chinese Han patients with essential tremor
F-Box Only Protein 7 Gene in Parkinsonian-Pyramidal Disease
Novel ATPase Cu2+ Transporting Beta Polypeptide Mutations in Chinese Families with Wilson's
短指/趾的分子遗传学研究进展
Genetic analysis of the FBXO42 gene in Chinese Han patients with Parkinson's disease
The role of FUS gene variants in neurodegenerative diseases
遗传性肾炎的遗传学研究进展
甲状腺髓样癌遗传学研究进展
The Molecular Biology of Genetic-Based Epilepsies
VHL综合征遗传学研究
Genetic analysis of a Chinese Han family with multiple endocrine neoplasia type 2A
Heterogeneous phenotype in a family with the FERM domain-containing 7 gene R335X mutation
屈曲指研究进展
Genetic analysis of the S100B gene in Chinese patients with Parkinson disease
Genetic analysis of the FBXO48 gene in Chinese Han patients with Parkinson disease
Identification of a GJA3 mutation in a Chinese family with congenital nuclear cataract using exome s
The VPS35 gene and Parkinson’s disease
Genetics, Molecular Biology, and Phenotypes of X-Linked Epilepsy
Molecular genetics of congenital nuclear cataract
Genetic variants and animal models in SNCA and Parkinson disease
Genetic analysis of the fused in sarcoma gene in Chinese Han patients with Parkinson's disease
先天性耳前瘘管研究进展
Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using ex