Whole-exome sequencing identifies functional classes of gene mutations associated with bone marrow failure in pediatric Fanconi Anemia patients

Eur J Haematol. 2021 Aug;107(2):293-294. doi: 10.1111/ejh.13645. Epub 2021 May 24.
No abstract available

Publication types

  • Letter

MeSH terms

  • Bone Marrow Failure Disorders / etiology
  • Bone Marrow Failure Disorders / genetics*
  • Cell Movement / genetics
  • Child
  • Exome Sequencing*
  • Fanconi Anemia / complications
  • Fanconi Anemia / genetics*
  • Gene Ontology
  • Genomic Instability / genetics*
  • Humans
  • Mitosis / genetics
  • Mutation*
  • Protein Transport / genetics
  • Thumb / abnormalities