Human Genome Epidemiology Literature Finder
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Query Trace: Cerebellar Ataxia and ATXN10[original query] |
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Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation. Neuromolecular medicine 2017 9 19 (4): 501-509. Bampi Giovana B, Bisso-Machado Rafael, Hünemeier Tábita, Gheno Tailise C, Furtado Gabriel V, Veliz-Otani Diego, Cornejo-Olivas Mario, Mazzeti Pillar, Bortolini Maria Cátira, Jardim Laura B, Saraiva-Pereira Maria Luiza, |
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