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Congenital dyserythropoietic anemia type 1: a case with novel compound heterozygous mutations in the C15orf41 gene.

Jan PalmbladBirgitta SanderBarbaraJ J BainMonika KlimkowskaErik Björck
Published in: American journal of hematology (2018)
Keyphrases
  • chronic kidney disease
  • early onset
  • copy number
  • genome wide
  • iron deficiency
  • gene expression
  • transcription factor