Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly

Clin Genet. 2011 Mar;79(3):296-9. doi: 10.1111/j.1399-0004.2010.01544.x.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Child
  • Dyrk Kinases
  • Female
  • Gene Deletion*
  • Genetic Association Studies
  • Heterozygote
  • Humans
  • Infant
  • Intellectual Disability / genetics*
  • Male
  • Microcephaly / genetics*
  • Phenotype
  • Protein Serine-Threonine Kinases / genetics*
  • Protein-Tyrosine Kinases / genetics*

Substances

  • Protein-Tyrosine Kinases
  • Protein Serine-Threonine Kinases