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]

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Author List

  • Chapleau CA; Lane J; Kirwin S; Schanen C; Vinette KMB; Stubbolo D; Macleod P; Glaze DG; Motil KJ; Neul JL
  • Start Page

  • 1346
  • Volume

  • 164
  • Issue

  • 5