Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and THAP1[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 |
SGCE mutations cause psychiatric disorders: clinical and genetic characterization. Brain : a journal of neurology 2013 Jan 136 (Pt 1): Pt 1. Peall KJ, Smith DJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, Smith M, Whone A, Pall H, White C, Lux A, Jardine P, Bajaj N, Lynch B, Kirov G, O'Riordan S, Samuel M, Lynch T, King MD, Chinnery PF, Warner TT, Blake DJ, Owen MJ, Morris HR |
Intracranial calcifications and dystonia associated with a novel deletion of chromosome 8p11.2 encompassing SLC20A2 and THAP1. BMJ case reports 2019 5 12 (5): . Mu Weiyi, Tochen Laura, Bertsch Caroline, Singer Harvey S, Barañano Kristin |
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 |
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- Page last updated:Apr 22, 2024
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