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Mutations and polymorphisms in the human methyl CpG-binding protein MECP2
Authors:Miltenberger-Miltenyi Gabriel  Laccone Franco
Affiliation:1. Institute of Human Genetics, University of G?ttingen, G?ttingen, Germany;2. Institute of Human Genetics, University of G?ttingen, G?ttingen, GermanyInstitute of Human Genetics, University of G?ttingen, Heinrich‐Düker‐Weg 12, D‐37073, G?ttingen, Germany
Abstract:
Keywords:Rett syndrome  RTT  RS  MECP2  mutation screening  mental retardation, X‐linked
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