
doi: 10.1007/bf02904841
pmid: 6622930
A case of congenital afibrinogenemia is described. In the family studied, the defect is transmitted as an autosomal recessive trait. The possible heterogeneity of congenital afibrinogenemia is discussed.
Adult, Humans, Female, Afibrinogenemia, Pedigree
Adult, Humans, Female, Afibrinogenemia, Pedigree
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