Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia

Br J Haematol. 2013 Feb;160(4):559-61. doi: 10.1111/bjh.12134. Epub 2012 Nov 28.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Bone Marrow Diseases / genetics*
  • Child
  • Child, Preschool
  • Exocrine Pancreatic Insufficiency / genetics*
  • Female
  • Heterozygote
  • Humans
  • Infant
  • Infant, Newborn
  • Leukemia, Myeloid, Acute / genetics*
  • Lipomatosis / genetics*
  • Male
  • Mutation / genetics*
  • Proteins / genetics*
  • Shwachman-Diamond Syndrome

Substances

  • Proteins
  • SBDS protein, human