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

Identification of six novel F9 mutations among haemophilia B patients from Macedonia and Bulgaria.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Mar 2015

Sukarova Stefanovska E P, Bozinovski G, Trajkova-Antevska Z, Dejanova-Ilijevska V, Petkov G, Plaseska-Karanfilska D A

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 Amino Acid Sequence
Share to Amino Acid Substitution
Share to Bulgaria
Share to Exons

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Factor IX

Share to Hemophilia B

Share to Mutation

Source

Identifiers

PMID: 25582609
DOI: 10.1111/hae.12620

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of six novel F9 mutations among haemophilia B patients from Macedonia and Bulgaria.PMID 25582609Read ↗

Spectrum of F8 gene mutations in haemophilia A patients from Slovenia.Semantic proximity Read ↗

The <scp>CDC</scp> Hemophilia B mutation project mutation list: a new online resourceSemantic proximity Read ↗

Novel F8 and F9 gene variants from the PedNet hemophilia registry classified according to ACMG/AMP guidelines.Semantic proximity Read ↗

F9 mutations causing deletions beyond the serine protease domain confer higher risk for inhibitor development in hemophilia B.Semantic proximity Read ↗

Molecular analysis of severe hemophilia B in Indian families: Identification of mutational hotspot and novel variants.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: F9. Disease: Haemophilia B.Semantic proximity Read ↗

Principles of genetic variations and molecular diseases: applications in hemophilia A.Semantic proximity Read ↗

Mutation Spectrum and Genotype-Phenotype Analyses in a Pakistani Cohort With Hemophilia B.Semantic proximity Read ↗

The Canadian "National Program for hemophilia mutation testing" database: a ten-year review.Semantic proximity Read ↗

Assessment of the F9 genotype-specific FIX inhibitor risks and characterisation of 10 novel severe F9 defects in the first molecular series of Argentinian patients with haemophilia B.Semantic proximity Read ↗

Five novel factor IX mutations in unrelated hemophilia B patients.Semantic proximity Read ↗

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition.Semantic proximity Read ↗

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