Deletion of CUL4B leads to concordant phenotype in a monozygotic twin pair

Clin Genet. 2012 Sep;82(3):292-4. doi: 10.1111/j.1399-0004.2011.01839.x. Epub 2012 Jan 11.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adolescent
  • Cullin Proteins / genetics*
  • Diseases in Twins / genetics*
  • Gene Deletion*
  • Humans
  • Male
  • Phenotype*
  • Twins, Monozygotic / genetics*

Substances

  • CUL4B protein, human
  • Cullin Proteins