Associated Papers
Congenital fibrinogen disorders: Strengthening genotype-phenotype correlations through novel genetic diagnostic tools.
Ramanan R et al.
British Journal of Haematology, 2023
Cortical atrophy and hypofibrinogenemia due to FGG and TBCD mutations in a single family: a case report.
Stephen J et al.
Bmc Medical Genetics, 2018
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