Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Movement Disorders and C9orf72[original query] |
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C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies. Neurology 2014 Jan 82 (4): 292-9. Hensman Moss Davina J, Poulter Mark, Beck Jon, Hehir Jason, Polke James M, Campbell Tracy, Adamson Garry, Mudanohwo Ese, McColgan Peter, Haworth Andrea, Wild Edward J, Sweeney Mary G, Houlden Henry, Mead Simon, Tabrizi Sarah |
A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing. Movement disorders : official journal of the Movement Disorder Society 2019 2 34 (4): 506-515. Lin Chin-Hsien, Chen Pei-Lung, Tai Chun-Hwei, Lin Hang-I, Chen Chih-Shan, Chen Meng-Ling, Wu Ruey-Me |
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