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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: May 31, 2023. (Total: 217454Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Factor V Deficiency and F7[original query]
F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency. Results from a genotype-phenotype study.
Thrombosis and haemostasis 2017 Apr .
Quintavalle Gabriele, Riccardi Federica, Rivolta Gianna Franca, Martorana Davide, Di Perna Caterina, Percesepe Antonio, Tagliaferri Annarita,
[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].
Zhongguo shi yan xue ye xue za zhi 2018 4 26 (2): 508-515.
Liu Shan, Zhang Jing-Yu, Li Zheng-Rong, Wang Yan, Niu Zhi-Yun, Lin Feng-
Next-generation sequencing and recombinant expression characterized aberrant splicing mechanisms and provided correction strategies in factor VII deficiency.
Haematologica 2019 7 105 (3): 829-837.
Ferraresi Paolo, Balestra Dario, Guittard Caroline, Buthiau Delphine, Pan-Petesh Brigitte, Maestri Iva, Farah Roula, Pinotti Mirko, Giansily-Blaizot Muri
Clinical phenotype and F7 gene genotype in 40 Tunisian patients with congenital factor VII deficiency.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2022 7 33 (5): 280-284.
Ouardani Cherifa, Elmahmoudi Hejer, ELborgi Wejden, Gharbi Maroua, Meriem Achour, Gouider Em
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