Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome

Leukemia. 2017 Aug;31(8):1827-1830. doi: 10.1038/leu.2017.142. Epub 2017 May 10.
No abstract available

Publication types

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

MeSH terms

  • Child, Preschool
  • Chromosomes, Human, Pair 7*
  • Female
  • Germ-Line Mutation*
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Male
  • Monosomy*
  • Myelodysplastic Syndromes / genetics*
  • Proteins / genetics*
  • Siblings*

Substances

  • Intracellular Signaling Peptides and Proteins
  • Proteins
  • SAMD9 protein, human