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Molecular Network Analysis Suggests a Logical Hypothesis for the Pathological Role of C9orf72 in Amyotrophic Lateral Sclerosis/Frontotemporal Dementia

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Background Expanded GGGGCC hexanucleotide repeats. ranging from hundreds to thousands in number. located in the noncoding region of the chromosome 9 open reading frame 72 ( C9orf72 ) gene represent the most common genetic abnormality for familial and sporadic amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) (abbreviated as C9ALS). Currently. https://www.lightemupsequences.com/hot-mega-Esko-Nexus-HeightMaster-Vented-Safety-Helmet-big-savings/
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