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

Mutations of human butyrylcholinesterase gene in a family with hypocholinesterasemia.

Human mutation - 1 Jan 1995

Iida S, Kinoshita M, Fujii H, Moriyama Y, Nakamura Y, Yura N, Moriwaki K

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 Butyrylcholinesterase
Share to Hypercholesterolemia
Share to Molecular Sequence Data

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

Share to Mutation

Share to Pedigree

Share to Polymorphism, Single-Stranded Conformational

Source

Identifiers

PMID: 8680411
DOI: 10.1002/humu.1380060411

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

Mutations of human butyrylcholinesterase gene in a family with hypocholinesterasemia.PMID 8680411Read ↗

Proposed nomenclature for human butyrylcholinesterase genetic variants identified by DNA sequencing.Semantic proximity Read ↗

Butyrylcholinesterase Atypical Mutation in a Patient Undergoing Electroconvulsive Therapy.Semantic proximity Read ↗

A pregnant woman with genetic variants of butyrylcholinesterase and inflammatory bowel disease.Semantic proximity Read ↗

Genetic mutations affecting human lipoproteins, their receptors, and their enzymes.Semantic proximity Read ↗

[Gene mutations responsible for hyperlipoproteinemia].Semantic proximity Read ↗

[Gene mutations in familial hyperlipidemias].Semantic proximity Read ↗

Discovery of a new function of human butyrylcholinesterase and the catalytic activity of its natural variants toward homocysteine thiolactone hydrolysisSemantic proximity Read ↗

Genetic mutations causing hereditary cholestasis.Semantic proximity Read ↗

Novel mutation and multiple mutations found in the human butyrylcholinesterase gene.Semantic proximity Read ↗

Genetic mutations of butyrylcholine esterase identified from phenotypic abnormalities in Japan.Semantic proximity Read ↗

Phenotypic and molecular biological analysis of human butyrylcholinesterase variants.Semantic proximity Read ↗

[Gene mutations in the enzymes involved in lipid metabolism].Semantic proximity Read ↗

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