Fibrinogen storage disease in a Chinese boy with de novo fibrinogen Aguadilla mutation: Incomplete response to carbamazepine and ursodeoxycholic acid

Overview of attention for article published in BMC Gastroenterology, August 2016

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Congenital hypofibrinogenemia

Cited by user Joflaher on 12 Sep 2017

Congenital hypofibrinogenemia is a rare disorder in which one of the two genes responsible for producing fibrinogen, a critical blood clotting factor, is unable to make…

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