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

Familial early-onset deep venous thrombosis associated with a novel HRG mutation.

European journal of medical genetics - 1 Feb 2018

Luo Junfu, Zhang Wenwen, Zeng Qingfu, Zhou Weimin, Cao Qing, Zhou Wei

Abstract excerpt

Deep venous thrombosis (DVT) remains a serious clinical problem that affects millions of people worldwide. Some DVT cases are caused by inherited thrombophilia derived from genetic aberrations and several disease-causing genes have been identified so far. Among them, HRG is an uncommon one with limited related reports. Here, we reported on a family with early-onset DVT where acquired risky conditions were...

Read the complete abstract on PubMed

Topics

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

Share to Heterozygote
Share to Mutation
Share to Pedigree

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

Share to Proteins

Share to Venous Thrombosis

Source

Identifiers

PMID: 29108964
DOI: 10.1016/j.ejmg.2017.10.019

Genes

HRG

Variants

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

Familial early-onset deep venous thrombosis associated with a novel HRG mutation.PMID 29108964Read ↗

Curated disease‐causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTHSemantic proximity Read ↗

Favourable outcome of multisystem venous thrombosis associated with novel SERPINC1 mutation after treated with dabigatran: a case report and literature reviewSemantic proximity Read ↗

[Diagnosis and management of early-onset thrombophilia/thrombosis: a review].Semantic proximity Read ↗

Genetics of Venous Thrombosis: update in 2015.Semantic proximity Read ↗

Venous thromboembolic disease genetics: from variants to function.Semantic proximity Read ↗

What is currently known about the genetics of venous thromboembolism at the dawn of next generation sequencing technologies.Semantic proximity Read ↗

Congenital Hypodysfibrinogenemia due to γ326Cys→Tyr Mutation: Third Ever-Described Case Associated with Recurrent Venous Thrombosis and COVID Vaccine.Semantic proximity Read ↗

Genetic variations and their influence on risk and treatment of venous thrombosis.Semantic proximity Read ↗

High Prevalence of F2 20210G > A in Splanchnic Vein Thrombosis and Cerebral Venous Sinus Thrombosis: A Retrospective Cohort Study of Patients with Thrombosis in Atypical Sites.Semantic proximity Read ↗

[Advances in the genetics of venous thromboembolic disease].Semantic proximity Read ↗

Complexity and diversity of F8 genetic variations in the 1000 genomes.Semantic proximity Read ↗

Management of rare inherited bleeding disorders: Proposals of the French Reference Centre on Haemophilia and Rare Coagulation Disorders.Semantic proximity Read ↗

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