Associated Papers
Heterogeneity of congenital afibrinogenemia, from epidemiology to clinical consequences and management.
Casini A et al.
Blood Reviews, 2021
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
Molecular pathology of rare bleeding disorders (RBDs) in India: a systematic review.
Kulkarni BP et al.
Plos One, 2014
Molecular basis of quantitative fibrinogen disorders in 27 patients from India.
Sumitha E et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2013
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