MECP2 Mutation in a Boy With Language Disorder and Schizophrenia

This publication has 4 references indexed in Scilit:

• MECP2 mutation in male patients with non‐specific X‐linked mental retardation
  Published by Wiley ,2000
• Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males
  The Lancet, 2000
• Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots
  American Journal of Human Genetics, 1999
• Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
  Nature Genetics, 1999