Associated Papers
[Congenital hypofibrinogenemia associated with a novel mutation in FGG gene].
Wang Y et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2015
Novel mutations (γTrp208Leu and γLys232Thr) leading to congenital hypofibrinogenemia in two unrelated Chinese families.
Zhu L et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2014
Select a paper to view details