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Erratum to Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in rett syndrome [Am J Med Genet Part A, 161A, (2014) 1638-1646]

  • Author(s): Chapleau, CA
  • Lane, J
  • Kirwin, S
  • Schanen, C
  • Vinette, KMB
  • Stubbolo, D
  • Macleod, P
  • Glaze, DG
  • Motil, KJ
  • Neul, JL
  • Skinner, SA
  • Kaufmann, WE
  • Percy, AK
  • et al.

Published Web Location

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3689857/
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