Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The prevalence of heterozygous F12 mutations in Chinese population and its relevance to incidents of thrombosis.

BMC medical genetics - 27 Mar 2018

Wu Xi, Ding Qiulan, Wang Xuefeng, Dai Jing, Wu Wenman

Abstract excerpt

BACKGROUND: The contribution of moderate coagulation factor XII (FXII) deficiency to development of thromboembolism is still undetermined. We have tried to show the relevance of FXII deficiency to incidences of venous thrombosis by exploring the prevalence of F12 gene mutations in Chinese patients with thrombotic disorders. METHODS: One hundred and six patients with venous thromboembolism (VTE) and 220 healthy...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Asian People
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Factor XII

Share to Heterozygote

Share to Incidence

Share to Venous Thrombosis

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 29587641
DOI: 10.1186/s12881-018-0557-1
PMCID: PMC5870241

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The prevalence of heterozygous F12 mutations in Chinese population and its relevance to incidents of thrombosis.PMID 29587641Read ↗

Novel Insights into Heterozygous Factor XIII Deficiency.Semantic proximity Read ↗

Clinical manifestations and mutation spectrum of 57 subjects with congenital factor XI deficiency in China.Semantic proximity Read ↗

Clinical and genetic spectrum of factor XII deficiency in the Han population of East China.Semantic proximity Read ↗

Genetic analysis in Factor XI deficient patients from central China: identification of one novel and seven recurrent mutations.Semantic proximity Read ↗

Factor XII deficiency: a clinical and molecular genetic study.Semantic proximity Read ↗

Clinical characteristics and genetic variant spectrum of 27 patients with coagulation factor XI deficiency.Semantic proximity Read ↗

Molecular Basis of Congenital Factor XIII Deficiency in Iran.Semantic proximity Read ↗

Factor VII deficiency in China: Phenotype, genotype and current status of management.Semantic proximity Read ↗

Congenital factor XI deficiency, complete genotype and phenotype of two Iranian families.Semantic proximity Read ↗

Prevalence of the Factor XIII Val34Leu Polymorphism in Korean Patients with Deep Vein Thrombosis.Semantic proximity Read ↗

Double Heterozygous Mutations (Cys247Tyr and 252delAsn) Cause Factor XII Deficiency in a Chinese Family.Semantic proximity Read ↗

A Novel Homozygous Missense Mutation (Ile583Asn) in a Consanguineous Marriage Family with Hereditary Factor XII Deficiency: A Case Report.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.