Associated Papers
The spectrum of factor XI deficiency in Southeast China: four recurrent variants can explain most of the deficiencies.
Zhang K et al.
Orphanet Journal of Rare Diseases, 2024
A novel mutation (Leu60Pro) in a Chinese pedigree with hereditary factor XI deficiency.
Xie H et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2021
[A family with hereditary FⅪ deficiency caused by compound heterozygous mutation].
Zheng XY et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2021
Select a paper to view details