Hepatic fibrinogen storage disease and hypofibrinogenemia caused by fibrinogen Aguadilla mutation: a case report.

Volume: 48, Issue: 1, Pages: 300060519898033 - 300060519898033
Published: Jan 22, 2020
Abstract
Hepatic fibrinogen storage disease is a rare autosomal dominant genetic disorder characterized by hypofibrinogenemia, as well as the retention of variant fibrinogen within the hepatocellular...
Paper Details
Title
Hepatic fibrinogen storage disease and hypofibrinogenemia caused by fibrinogen Aguadilla mutation: a case report.
Published Date
Jan 22, 2020
Volume
48
Issue
1
Pages
300060519898033 - 300060519898033
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