Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 4 (of 4 Records) |
Query Trace: Meige Syndrome[original query] |
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Novel THAP1 gene mutations in patients with primary dystonia from southwest China. Journal of the neurological sciences 2011 Oct 309 (1-2): 63-7. Song Wei, Chen Yongping, Huang Rui, Chen Ke, Pan Pinglei, Yang Yuan, Shang Hui-Fa |
[Clinical and genetic study of a family affected with spinocerebellar ataxia 3 and polycystic kidney disease]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2015 Feb 32 (1): 60-3. Li Haijiang, Zhang Linming, Chen Tao, Yang Dan, Zhu Yangfan, Wang Liho |
Genetic screening in patients of Meige syndrome and blepharospasm. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 1 43 (6): 3683-3694. Teng Xinqi, Qu Qiang, Shu Yi, Gong Jiaoe, Xu Bei, Qu Ji |
Association analyses between the variants of SNAP25, SV2C and ST3GAL2 and the efficacy of botulinum toxin A in the treatment of the primary Meige syndrome. Heliyon 2024 4 10 (8): e28543. Wen-Qi Wu, Kai Li, Lu-Lu Chu, Ting-Ting Shen, Yang Li, Ying-Ying Xu, Qi-Lin Zhang, Chun-Feng Liu, Jing Liu, Xu-Ping Zhou, Wei-Feng L |
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