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publicationName European journal of human genetics : EJHG
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bibliographicCitation Choquet K, Tétreault M, Yang S, La Piana R, Dicaire MJ, Vanstone MR, Mathieu J, Bouchard JP, Rioux MF, Rouleau GA; Care4Rare Canada Consortium, Boycott KM, Majewski J, Brais B. SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases. Eur J Hum Genet. 2016 Jul;24(7):1016–21. PMID: 26626314; PMCID: PMC5070891.
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title SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases
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