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C9orf72 hexanucleotide repeat expansion found in suspected spinobulbar muscular atrophy (SBMA).

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0 Published in 2022 at "Neurologia i neurochirurgia polska"

DOI: 10.5603/pjnns.a2022.0039

Abstract: INTRODUCTION The expansion of a hexanucleotide GGGGCC repeat (G4C2) in the C9orf72 locus is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). In addition, C9orf72 expansion has also been… read more here.

Keywords: hexanucleotide; atrophy sbma; repeat; muscular atrophy ... See more keywords