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A rare case of Glanzmann's thrombasthenia and factor VII deficiency due to a combination of pathogenic and non-pathogenic gene variants.

Rutuja DeshpandeSharda ShanbhagAnshul JadliShrimati Shetty
Published in: Haemophilia : the official journal of the World Federation of Hemophilia (2019)
Keyphrases
  • rare case
  • copy number
  • genome wide