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Neuroimaging features of C9ORF72 expansion

  • Author(s): Rosen, Howard
  • Yokoyama, JS
  • Rosen, HJ
  • et al.

Published Web Location

http://europepmc.org/articles/PMC3580454?pdf=render
No data is associated with this publication.
Abstract

Hexanucleotide expansion intronic to chromosome 9 open reading frame 72 (C9ORF72) has recently been identified as the most common genetic cause of both familial and sporadic amyotrophic lateral sclerosis and of frontotemporal dementia with or without conco

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