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

Analysis of Hereditary FXII Deficiency Caused by Three Mutations Including a Novel Mutation

Turkish journal of haematology : official journal of Turkish Society of Haematology - 1 Mar 2024

Ye Longying, Liu Meina, Yang Lihong, Wang Mingshan, Xie Yaosheng

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 XII
Share to Mutation
Share to Mutation, Missense

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Open in PubMed Open full text

Identifiers

PMID: 38298123
DOI: 10.4274/tjh.galenos.2024.2024.0016
PMCID: PMC10918392

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

Analysis of Hereditary FXII Deficiency Caused by Three Mutations Including a Novel MutationPMID 38298123Read ↗

Characterization of the genetic basis of FXI deficiency in two Turkish patients.Semantic proximity Read ↗

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

Genetic analysis of a pedigree with hereditary coagulation factor XII deficiencySemantic proximity Read ↗

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

Characterisation of five factor XI mutations.Semantic proximity Read ↗

Clinical manifestations and mutation spectrum of 57 subjects with congenital factor XI deficiency in China.Semantic proximity Read ↗

Seven novel point mutations in the F11 gene in Iranian FXI-deficient patients.Semantic proximity Read ↗

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

Factor XIII Deficiency: Laboratory, Molecular, and Clinical AspectsSemantic proximity Read ↗

Spectrum of factor X gene mutations in Iranian patients with congenital factor X deficiency.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 Congenital Factor XIII Deficiency in Iran.Semantic proximity Read ↗

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