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Author Report for: Proukakis C

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    Title: Genetic and phenotypic characterization of complex hereditary spastic paraplegia
    Kara E, Tucci A, Manzoni C, Lynch DS, Elpidorou M, Bettencourt C, Chelban V, Manole A, Hamed SA and Houlden H <19 more author(s)>
    Ref: Brain, 139:1904, 2016 : PubMed

            

    Title: Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia
    Simpson MA, Cross H, Proukakis C, Pryde A, Hershberger R, Chatonnet A, Patton MA, Crosby AH
    Ref: American Journal of Human Genetics, 73:1147, 2003 : PubMed

            


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