Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Dystonia and ATP1A3[original query] |
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Common polymorphisms in dystonia-linked genes and susceptibility to the sporadic primary dystonias. Parkinsonism & related disorders 2012 May 18 (4): 351-7. Newman Jeremy R B, Sutherland Greg T, Boyle Richard S, Limberg Nicole, Blum Stefan, O'Sullivan John D, Silburn Peter A, Mellick George |
Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2021 11 43 (4): 2555-2563. Wei Wen, Zheng Xiu-Fen, Ruan Dan-Dan, Gan Yu-Mian, Zhang Yan-Ping, Chen Ying, Lin Xin-Fu, Tang Fa-Qiang, Luo Jie-Wei, Li Yun-F |
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