Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome.

Academic Article

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Digital Object Identifier (doi)

Author List

  • Amir RE; Fang P; Yu Z; Glaze DG; Percy AK; Zoghbi HY; Roa BB; Van den Veyver IB
  • Volume

  • 42
  • Issue

  • 2