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Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias

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author: Isabelle Leber  Claudia Cagnoli  Cecilia Mancini  Patrizia Pappi  Alexandra Durr  Sylvie Forlani  Giovanni Stevanin  Cécile Zaros  Alexis Brice  Alfredo Brusco  Nicola Migone  Pascale Ribai 

Publication date October 1, 2010
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