Associated Papers
Hereditary protein C deficiency caused by compound heterozygous mutants in two independent Chinese families.
Wu YT et al.
Pathology, 2014
Different impact of two mutations of a novel compound heterozygous protein C deficiency with late onset thrombosis.
Yang LH et al.
Genetics and Molecular Research : Gmr, 2014
[Molecular mechanisms of Glanzmann thrombasthenia caused by alpha II b L721R and Q860X compound heterozygous mutation].
Shen WZ et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2008
[Severe hereditary coagulation factor V deficiency caused by two novel heterozygous mutations].
Zhou RF et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2005
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