Associated Papers
Development of Engineered-U1 snRNA Therapies: Current Status.
Gonçalves M et al.
International Journal of Molecular Sciences, 2023
A thrombophilic allele of clotting Factor VII/VIIa promoting recurrent pulmonary emboli, clinical details, and a structural model of the altered protein: a case report.
Newman K et al.
Journal of Medical Case Reports, 2023
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
Pankratz N et al.
Human Molecular Genetics, 2022
Novel heterozygous F7 gene mutation (c. C1286T) associated with congenital factor VII deficiency: A case report and literature review.
Tang H et al.
Journal of Clinical Laboratory Analysis, 2022
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency.
Neerman-Arbez M et al.
Blood, 1999
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