Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: preliminary data suggest an involvement of epigenetic mechanisms

Am J Med Genet A. 2009 Oct;149A(10):2306-10. doi: 10.1002/ajmg.a.32990.
No abstract available

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Case-Control Studies
  • Child
  • Child Development Disorders, Pervasive / genetics
  • Child, Preschool
  • Developmental Disabilities / genetics*
  • Epigenesis, Genetic / physiology*
  • Fragile X Mental Retardation Protein / genetics*
  • Gene Frequency
  • Genetic Linkage
  • Humans
  • Male
  • Trinucleotide Repeat Expansion / genetics*
  • Young Adult

Substances

  • FMR1 protein, human
  • Fragile X Mental Retardation Protein