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

Shiyu WangNatalia H ZbibAlyza SkaistJiang GuiRafael Madero-MarroquinFederico De MarchiLukasz P GondekWilliam MatsuiBonnie W Lau
Published in: European journal of haematology (2021)
Keyphrases
  • bone marrow
  • end stage renal disease
  • chronic kidney disease
  • ejection fraction
  • newly diagnosed
  • mesenchymal stem cells
  • prognostic factors
  • genome wide
  • young adults
  • iron deficiency