A novel deletion-insertion mutation identified in exon 3 of FXN in two siblings with a severe Friedreich ataxia phenotype Journal Articles Refereed uri icon

Overview

Published in

  • Neurogenetics

Time

Date/time value

  • 2011

Identity

Digital Object Identifier (DOI)

  • 10.1007/s10048-011-0296-3

Additional Document Info

Parent Title

  • NEUROGENETICS

Volume

  • 12

Issue

  • 4

Publisher

  • Springer
  • External Links
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