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 diagnosis of inherited coagulation disorders--sequence analysis of hemophilia B patients with anti-factor IX antibodies].

Rinsho byori. The Japanese journal of clinical pathology - 1 Sept 1990

Tanimoto M, Matsushita T, Takamatsu J, Saito H

Abstract excerpt

Seven hemophilia B patients with anti-factor IX antibodies are studied with molecular means. A total factor IX gene deletion was detected in four patients from three distinct families. Three other patients without detectable gene arrangements were investigated at the DNA sequence level. Enzymatic...

Topics

Antibodies
Base Sequence
Blotting, Southern
Factor IX
Hemophilia B
Humans
Mutation
Polymerase Chain Reaction

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 2232265

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-2232265-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Molecular diagnosis of inherited coagulation disorders--sequence analysis of hemophilia B patients with anti-factor IX antibodies].PMID 2232265Read ↗

DNA sequence analysis of three inhibitor-positive hemophilia B patients without gross gene deletion: identification of four novel mutations in factor IX gene.Semantic proximity Read ↗

[Coagulation factor IX gene mutations of ten patients with hemophilia B].Semantic proximity Read ↗

[Mutational Analysis of Hemophilia B in Russia: Molecular-Genetic Study].Semantic proximity Read ↗

[Molecular analysis of hemophilia A].Semantic proximity Read ↗

Factor IX gene analysis in 70 unrelated patients with haemophilia B: description of 13 new mutations.Semantic proximity Read ↗

[Molecular diagnosis of haemophilia A in clinical practice].Semantic proximity Read ↗

[Molecular genetics of hemophilia A].Semantic proximity Read ↗

Molecular diagnostics of 15 hemophilia A patients: characterization of eight novel mutations in the factor VIII gene, two of which result in exon skipping.Semantic proximity Read ↗

[Gene diagnosis of 3 haemophilia B families].Semantic proximity Read ↗

Molecular analysis of hemophilia B in Poland: 12 novel mutations of the factor IX gene.Semantic proximity Read ↗

Haemophilia B caused by a point mutation in a donor splice junction of the human factor IX gene.Semantic proximity Read ↗

[Molecular analysis of two pedigrees with inherited coagulation factor VII deficiency].Semantic proximity Read ↗

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