Associated Papers
Computational analysis of the functional and structural impact of the most deleterious missense mutations in the human Protein C.
Farajzadeh-Dehkordi M et al.
Plos One, 2023
Genotype-Phenotype Relationships in a Large French Cohort of Subjects with Inherited Protein C Deficiency.
Alhenc-Gelas M et al.
Thrombosis and Haemostasis, 2020
Identification of 58 Mutations (26 Novel) in 94 of 109 Symptomatic Spanish Probands with Protein C Deficiency.
Martos L et al.
Thrombosis and Haemostasis, 2019
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