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- W2776523598 abstract "C9ORF72 gene mutation on chromosome 9 corresponding to a repetition of hexanucleotides (GGGGCC) xn is the most common mutation found in frontotemporal lobar dementia (FTLD) and amyotrophic lateral sclerosis (SLA) [1]." @default.
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- W2776523598 date "2017-01-24" @default.
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- W2776523598 title "Case Report: Extent of the Clinical Spectrum for C9orf72 Mutation - From Frontotemporal Dementia to Autonomic Dysfunction" @default.
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- W2776523598 doi "https://doi.org/10.17352/aggr.000004" @default.
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