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

[Congenital FⅦ Deficiency Associated with a Novel Mutation in F7 Gene].

Zhongguo shi yan xue ye xue za zhi - 1 Jun 2024

Wang Ying-Yu, Zhang Yong-Gen, Chen Wen-Bai

Abstract excerpt

OBJECTIVE: To identify the genetic mutation of coagulation factor Ⅶ ( F7) gene in a pedigree with coagulation factor Ⅶ (FⅦ) deficiency and explore the molecular pathogenesis. METHODS: The prothrombin time (PT), activated partial thromboplastin time (APTT), thrombin time (TT), D-dimer (DD), fibrin degradation products (FDP) and coagulation factor Ⅶ activity (FⅦ:C) of the proband and her family members were...

Read the complete abstract on PubMed

Topics

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

Share to Exons
Share to Factor VII
Share to Factor VII Deficiency

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heterozygote

Share to Mutation

Share to Pedigree

Source

Identifiers

PMID: 38926980
DOI: 10.19746/j.cnki.issn.1009-2137.2024.03.032

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Congenital FⅦ Deficiency Associated with a Novel Mutation in F7 Gene].PMID 38926980Read ↗

[Analysis of Phenotype and Genotype of A Family with Hereditary Coagulation Factor Ⅴ Deficiency Caused by A Compound Heterozygous Mutation].Semantic proximity Read ↗

[Analysis of A Pedigree with Hereditary Coagulation Factor Ⅻ Deficiency Caused by Compound Heterozygous Mutations].Semantic proximity Read ↗

[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].Semantic proximity Read ↗

[Phenotypic and mutational analysis of a pedigree affected with hereditary coagulation factor Ⅴ deficiency].Semantic proximity Read ↗

[Analysis of a Chinese pedigree affected with hereditary factor VII deficiency caused by compound heterozygous variants of F7 gene].Semantic proximity Read ↗

[Analysis of three Chinese pedigrees affected with Hereditary factor Ⅶ deficiency due to compound heterozygous variants of F7 gene].Semantic proximity Read ↗

[Phenotype and Genotype Analysis in Two Pedigrees with Hereditary Coagulation Factor Ⅺ Deficiency].Semantic proximity Read ↗

Analysis of clinical manifestations and molecular pathogenesis of six patients with hereditary blood coagulation factor VII deficiency.Semantic proximity Read ↗

[Genotype and phenotype analysis of congenital coagulator factor VII deficiency in four Chinese pedigrees].Semantic proximity Read ↗

[Analysis of Clinical Features and Gene Mutation in Children with Hereditary Coagulation Factor Deficiency].Semantic proximity Read ↗

[Analysis on the novel compound heterozygous mutation FⅪ of a patient with hereditary factor Ⅺ deficiency].Semantic proximity Read ↗

[Molecular analysis of two pedigrees with inherited coagulation factor VII deficiency].Semantic proximity Read ↗

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