Factor Vii Deficiency
What's New
Last Posted: Jan 18, 2024
- Genotype-Phenotype Relationship among 785 Unrelated White Women with Inherited Congenital Factor VII Deficiency: A Three-Center Database Study.
Susan Halimeh, et al. Journal of clinical medicine 2024 0 (1) - Interleukin 10, but not tumor necrosis factor-alpha, gene variations are associated with factor VII inhibitor development.
Nahid Ramezanpour, et al. Laboratory medicine 2023 0 - Factor VII deficiency: a novel missense variant and genotype-phenotype correlation in patients from Southern Italy.
Tiscia Giovanni, et al. Human genome variation 2017 0 17048 - [Analysis of Phenotype and L12R Mutation in Signal Peptide and 3' Non-translation Region c11814-insAA Mutation of F7 Gene in a Family with Hereditary Coagulation Factor VII Deficiency].
Liu Shan, et al. Zhongguo shi yan xue ye xue za zhi 2018 0 (2) 508-515 - Homozygous congenital factor VII deficiency with a novel mutation, associated with severe spontaneous intracranial bleeding in a neonate.
Kader Sebnem, et al. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2018 0 (5) 476-480 - Next-generation sequencing and recombinant expression characterized aberrant splicing mechanisms and provided correction strategies in factor VII deficiency.
Ferraresi Paolo, et al. Haematologica 2019 0 (3) 829-837 - Clinical phenotype and F7 gene genotype in 40 Tunisian patients with congenital factor VII deficiency.
Ouardani Cherifa, et al. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2022 0 (5) 280-284 - Recurrent mutations and genotype-phenotype correlations in hereditary factor VII deficiency in Korea.
Kwon Min-Jung, et al. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2011 0 (2) 102-5 - Vena porta thrombosis in patient with inherited factor VII deficiency.
Klovaite Jolanta, et al. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2010 0 (3) 285-8 - Molecular analysis of the genotype-phenotype relationship in factor VII deficiency.
Millar D S, et al. Human genetics 2000 0 (4) 327-42
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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