Associated Papers
Genotype-Phenotype Relationship among 785 Unrelated White Women with Inherited Congenital Factor VII Deficiency: A Three-Center Database Study.
Halimeh S et al.
Journal of Clinical Medicine, 2023
38202056 (PubMed )
Supplement: jcm-13-00049-s001.zip › jcm-2671474-supplementary.pdf
Utility of ACMG classification to support interpretation of molecular genetic test results in patients with factor VII deficiency.
Alesci RS et al.
Frontiers in Medicine, 2023
37521340 (PubMed )
Supplement: Table_2.pdf
Factor VII deficiency and the FVII mutation database.
McVey JH et al.
Human Mutation, 2001
Twenty two novel mutations of the factor VII gene in factor VII deficiency.
Wulff K et al.
Human Mutation, 2000
Molecular biology and clinical manifestation of hereditary factor VII deficiency.
Herrmann FH et al.
Seminars in Thrombosis and Hemostasis, 2000
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