Search Results - Charlesworth, Gavin

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    Delineating the phenotype of autosomal-recessive HPCA mutations: not only isolated dystonia! by Balint, Bettina (Author) , Charlesworth, Gavin (Author) , Erro, Roberto (Author) , Wood, Nicholas W. (Author) , Bhatia, Kailash P. (Author) ,


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    SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy by Charlesworth, Gavin (Author) , Balint, Bettina (Author) ,


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