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

A protein C and plasminogen compound heterozygous mutation and a compound heterozygote of protein C in two related Chinese families.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Oct 2016

Cheng Xiaoli, Wang Mingshan, Jiang Minghua, Bhugul Pravin A, Hao Xiuping, Yang Lihong

Abstract excerpt

Hereditary protein C (PC) deficiency and congenital plasminogen (PLG) deficiency are both factors of thrombophilia which were caused by PC and PLG gene mutations with the characteristics of activity and antigen decreasing inconsonantly. To illustrate the connection between gene mutations and the corresponding deficiencies of PC and PLG, we studied two related cases. The proband 1 showed a cranial venous sinus...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Child

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

Share to PROC gene

Share to Heterozygote

Share to Mutation

Share to Plasminogen

Share to Protein C

Share to Protein C Deficiency

Source

Identifiers

PMID: 27314862
DOI: 10.1097/MBC.0000000000000579

Genes

PLG
PROC

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

A protein C and plasminogen compound heterozygous mutation and a compound heterozygote of protein C in two related Chinese families.PMID 27314862Read ↗

Two novel compound heterozygous mutations associated with types I and II protein C deficiency with unusual phenotypes.Semantic proximity Read ↗

Molecular and clinical characterization of two independent Chinese families with protein C deficiencySemantic proximity Read ↗

[Clinical phenotype and gene mutation analysis of 12 patients with hereditary protein C deficiency in different families].Semantic proximity Read ↗

Two heterozygous mutations associated with type I protein C deficiency in two Chinese independent families.Semantic proximity Read ↗

Analysis of four hereditary protein C deficiencies associated with vascular thromboembolism.Semantic proximity Read ↗

Analysis of Four Hereditary Protein C Deficiencies Associated with Vascular ThromboembolismSemantic proximity Read ↗

The significance of F139V mutation on thrombotic events in compound heterozygous and homozygous protein C deficiency.Semantic proximity Read ↗

Compound heterozygous protein C deficiency with pulmonary embolism caused by a novel PROC gene mutation: Case report and literature review.Semantic proximity Read ↗

[Phenotype and genetic mutation analysis of an inherited protein C deficiency pedigree].Semantic proximity Read ↗

Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutations.Semantic proximity Read ↗

Genetic background analysis of protein C deficiency demonstrates a recurrent mutation associated with venous thrombosis in Chinese population.Semantic proximity Read ↗

Clinical and genetic features of protein C deficiency in 23 unrelated Chinese patients.Semantic proximity Read ↗

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