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Abnormal bleeding phenotype for mild haemophilia B patients with the p.Ile112Thr variation on the gene for factor IX.

Céline RowPierre ChamouniClaire BergerAnne LienhartSandrine MeunierMathilde FretignyVincent DalibardMarie VipreyHervé ChambostVirginie BarbayJulien Bovet
Published in: Haemophilia : the official journal of the World Federation of Hemophilia (2020)
Keyphrases
  • copy number
  • genome wide
  • atrial fibrillation
  • genome wide identification
  • dna methylation