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Congenital fibrinogen disorders: Strengthening genotype-phenotype correlations through novel genetic diagnostic tools

Radha Ramanan1,2,3, James D McFadyen1,2,4, Andrew C Perkins1,2,3

  • 1Department of Haematology, Alfred Hospital, Melbourne, Victoria, Australia.

British Journal of Haematology
|August 16, 2023
PubMed

Keywords:
afibrinogenemiacongenital fibrinogen disordersdysfibrinogenemiagenotype-phenotype correlationhypodysfibrinogenemiahypofibrinogenemianex-generation sequencing

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