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Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD. [electronic resource] by
Producer: 20200622 In: Acta neuropathologica vol. 137
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Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. [electronic resource] by
Producer: 20190321 In: The Lancet. Neurology vol. 17
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