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 novel c.290G>A mutation in the Factor 11 gene in a Dutch Caucasian family with a Factor XI deficiency.

Thrombosis research - 1 Apr 2015

Mulder R, Croles F N, Lukens M V, Meijer K, Mulder A B

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 Factor XI
Share to Factor XI Deficiency
Share to Mutation
Share to White People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Young Adult

Source

Identifiers

PMID: 25618263
DOI: 10.1016/j.thromres.2015.01.014

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel c.290G>A mutation in the Factor 11 gene in a Dutch Caucasian family with a Factor XI deficiency.PMID 25618263Read ↗

Three Factor 11 Mutations Associated with Factor XI Deficiency in a Turkish Family.Semantic proximity Read ↗

Identification of a novel factor XI gene mutational event in a Dutch Caucasian family with inherited factor XI deficiency.Semantic proximity Read ↗

Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11.Semantic proximity Read ↗

Detection and Gene Mutation Analysis of Three Variations in Two Unrelated Chinese Hereditary Coagulation Factor XI Deficiency Families.Semantic proximity Read ↗

Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families.Semantic proximity Read ↗

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

Cys482Trp missense mutation in the coagulation factor XI gene (F11) in a Korean patient with factor XI deficiency.Semantic proximity Read ↗

High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla study.Semantic proximity Read ↗

Identification of five novel mutations in the factor XI gene (F11) of patients with factor XI deficiency.Semantic proximity Read ↗

Severe factor XI deficiency caused by compound heterozygosity for the type III mutation and a novel insertion in exon 9 (codons 324/325 +G).Semantic proximity Read ↗

A novel mutation with Ins C (882-883) of the factor X gene in a Taiwanese Chinese factor X-deficient family.Semantic proximity Read ↗

Coagulation factor XI: a database of mutations and polymorphisms associated with factor XI deficiency.Semantic proximity Read ↗

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