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

[Molecular mechanisms of antithrombin gene mutations in 3 pedigrees with hereditary antithrombin deficiency].

Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi - 1 Mar 2013

Sun Ling, Yu Zi-qiang, Wang Chao-rong

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Antithrombin III Deficiency
Share to Antithrombins
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Share to Phenotype

Source

Identifiers

PMID: 23683427
DOI: 10.3760/cma.j.issn.0253-2727.2013.03.016

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Molecular mechanisms of antithrombin gene mutations in 3 pedigrees with hereditary antithrombin deficiency].PMID 23683427Read ↗

[Phenotypic and genetic analysis of a pedigree with inherited antithrombin deficiency].Semantic proximity Read ↗

[Phenotypic and genetic analysis of two pedigrees affected with hereditary antithrombin deficiency].Semantic proximity Read ↗

The molecular genetics of antithrombin deficiency.Semantic proximity Read ↗

[Gene diagnosis of antithrombin deficiency and factor VII deficiency].Semantic proximity Read ↗

[Molecular mechanisms of antithrombin deficiency caused by novel double heterozygous mutations].Semantic proximity Read ↗

[Analysis of clinical features and genotype in an inherited coagulation factor Ⅶ deficiency pedigree].Semantic proximity Read ↗

[Molecular mechanisms of recurrent venous thrombosis in two pedigrees with type I antithrombin deficiency].Semantic proximity Read ↗

[Molecular basis of hereditary thrombophilia].Semantic proximity Read ↗

Molecular genetics of human antithrombin deficiency.Semantic proximity Read ↗

[Antithrombin resistance: a new mechanism of inherited thrombophilia].Semantic proximity Read ↗

Antithrombin: structure and function.Semantic proximity Read ↗

[Type I hereditary antithrombin deficiency due to C2757T heterozygotic mutation in antithrombin gene].Semantic proximity Read ↗

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