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

Five novel factor IX mutations in unrelated hemophilia B families.

Human molecular genetics - 1 May 1993

Chen S H, Schoof J M, Scott C R, Thompson A R

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 Base Sequence
Share to DNA
Share to DNA Mutational Analysis
Share to Factor IX

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

Share to Hemophilia B

Share to Mutation

Share to Point Mutation

Share to Sequence Deletion

Source

Identifiers

PMID: 8518801
DOI: 10.1093/hmg/2.5.599

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Five novel factor IX mutations in unrelated hemophilia B families.PMID 8518801Read ↗

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

Twenty-five novel mutations of the factor IX gene in haemophilia B.Semantic proximity Read ↗

Clinical significance of two mutations in the factor IX gene in a family with haemophilia B.Semantic proximity Read ↗

Haemophilia B and factor IX mutations.Semantic proximity Read ↗

Hemophilia B: molecular pathogenesis and mutation analysis.Semantic proximity Read ↗

Factor IX mutations: rapid, direct screening methods for 20 new families with hemophilia B.Semantic proximity Read ↗

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

A novel missense mutation in F9 gene causes hemophilia B in a family with clinical variability.Semantic proximity Read ↗

Haemophilia B Due to a De Novo Insertion of a Human-Specific Alu Subfamily Member within the Coding Region of the Factor IX GeneSemantic proximity Read ↗

An updated interactive database for 1692 genetic variants in coagulation factor IX provides detailed insights into hemophilia B.Semantic proximity Read ↗

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

A new hemophilia B mutation in the propeptide region of the FIX gene.Semantic proximity Read ↗

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