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Paper Report for: Scarlato_2017_J.Neurol_264_2021

Reference
Title: Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21
Scarlato M, Citterio A, Barbieri A, Godi C, Panzeri E, Bassi MT
Ref: Journal of Neurology, 264:2021, 2017 : PubMed

        


Related information
Gene_Locus : human-SPG21
Mutation : F40EfsX27_human-SPG21,

Citations formats
Scarlato M, Citterio A, Barbieri A, Godi C, Panzeri E, Bassi MT (2017)
Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21
Journal of Neurology 264: 2021-2023

Scarlato M, Citterio A, Barbieri A, Godi C, Panzeri E, Bassi MT (2017)
Journal of Neurology 264: 2021-2023


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