Article

Prevalence of Rare F5 Variants in General Population From Bosnia and Herzegovina

2021-05-05

Abstract excerpt

<title>Abstract</title> <p><bold>Background: </bold>Human gene <italic>F5,</italic> encoding coagulation factor V, was previously reported to be highly polymorphic. Apart from FV Leiden, an array of other rare variants has been detected in clinical practice and associated with thrombotic events, especially in cases when patient’s phenotype and FV Leiden genotype were not in agreement.<bold>Methods and Results: </...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: c267c02b-0e97-567e-892f-79307832763d
DOI: 10.21203/rs.3.rs-456810/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Prevalence of Rare F5 Variants in General Population From Bosnia and HerzegovinaDOI 10.21203/rs.3.rs-456810/v1Read

Prevalence of rare F5 variants in general population from Bosnia and Herzegovina.Semantic proximity Read

Population study of thrombophilic markers and pharmacogenetic markers of warfarin prevalence in Bosnia and HerzegovinaSemantic proximity Read

Factor 5 mutation profile in German patients with homozygous and heterozygous factor V deficiency.Semantic proximity Read

New and De Novo Biallelic Variant Associated With Owren's Disease: Precision Medicine in Blooding DisordersSemantic proximity Read

Frequency of thrombophilia associated genes. Population – based study.Semantic proximity Read

Prevalence of genetic prothrombotic risk factors: 1691G > A FV, 20210G > A PT and 677C > T MTHFR mutations in the Bosnian population.Semantic proximity Read

Prevalence of F5 1691G>A, F2 20210G>A, and MTHFR 677C>T polymorphisms in Bosnian women with pregnancy loss.Semantic proximity Read

A novel mutation (Ser951LeufsTer8) in F5 gene leads to hereditary coagulation factor V deficiency.Semantic proximity Read

[Phenotypic and genetic analysis of a pedigree affected with hereditary FV deficiency due to a novel deletional variant of F5 gene].Semantic proximity Read

[Identification of a novel variant of F5 gene in a consanguineous pedigree affected with inherited coagulation factor V deficiency].Semantic proximity Read

Population-based prevalence and mutational landscape of von Willebrand disease using large-scale genetic databasesSemantic proximity Read

Novel F8 and F9 gene variants from the PedNet hemophilia registry classified according to ACMG/AMP guidelines.Semantic proximity Read