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Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa Lesage, S; Condroyer, C; Hecham, N; Anheim, M; ... Brice, A 2011
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Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B Wiszniewski, W.; Fondaneche, M. C.; Lambert, N.; Masternak, Krzysztof; ... Lisowska-Grospierre, B. 2000