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 characterization of a novel mutation in the factor XIII A subunit gene associated with a severe defect and an adulthood diagnosis.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Mar 2007

Trigui N, Frère C, D'Ercole C, Chambost H, Chapuis N, Pouymayou C, Morange P, de Mazancourt P

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 Abortion, Habitual
Share to Factor XIII Deficiency
Share to Mutation

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

Share to Pregnancy

Share to Pregnancy Complications, Hematologic

Share to Pregnancy Outcome

Source

Identifiers

PMID: 17286781
DOI: 10.1111/j.1365-2516.2006.01432.x

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular characterization of a novel mutation in the factor XIII A subunit gene associated with a severe defect and an adulthood diagnosis.PMID 17286781Read ↗

Deficiency causing mutations and common polymorphisms in the factor XIII-A gene.Semantic proximity Read ↗

Characterisation of six novel A-subunit mutations leading to congenital factor XIII deficiency and molecular analysis of the first diagnosed patient with this rare bleeding disorder.Semantic proximity Read ↗

Genetic analysis in FXI deficient patients from northwestern Italy: three novel and one recurrent mutation.Semantic proximity Read ↗

Molecular characterization of a novel mutation in the factor XIII a subunit gene associated with a severe defect: importance of prophylactic substitution.Semantic proximity Read ↗

Inherited factor X deficiency: molecular genetics and pathophysiology.Semantic proximity Read ↗

Molecular and functional basis of hereditary factor IX defects.Semantic proximity Read ↗

Genetic basis of severe factor XIII deficiency in a large cohort of Indian patients: Identification of fourteen novel mutations.Semantic proximity Read ↗

Molecular basis of inherited factor XIII deficiency: identification of multiple mutations provides insights into protein function.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: F8. Disease: Haemophilia A.Semantic proximity Read ↗

Two females with distinct de novo missense pathogenic variants in MED12 and vastly differing phenotypes.Semantic proximity Read ↗

A pediatric genetic disorder diagnosed in adulthood.Semantic proximity Read ↗

An update of the mutation profile of Factor 13 A and B genes.Semantic proximity Read ↗

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