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

Frequent sequence variant in the human tyrosine hydroxylase gene.

Human genetics - 1 Jun 1995

Lüdecke B, Bartholomé K

Abstract excerpt

A polymorphism of human tyrosine hydroxylase changing the amino acid 81Val to 81Met is located in exon 2 of the human tyrosine hydroxylase gene.

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 Dystonia
Share to Gene Frequency
Share to Genetic Variation

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

Share to Molecular Sequence Data

Share to Point Mutation

Share to Tyrosine 3-Monooxygenase

Source

Identifiers

PMID: 7789962
DOI: 10.1007/BF00209496

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 · 8 closest

Frequent sequence variant in the human tyrosine hydroxylase gene.PMID 7789962Read ↗

Tyrosine hydroxylase Val-81-Met polymorphism associated with early-onset alcoholism.Semantic proximity Read ↗

A polymorphic synonymous mutation in human ornithine-delta-aminotransferase (N378N).Semantic proximity Read ↗

Dinucleotide repeat polymorphism at the human tyrosinase gene.Semantic proximity Read ↗

Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene (TH)Semantic proximity Read ↗

A trinucleotide deletion together with a base duplication event at codon 439 in the human tyrosinase gene identifies a mutational hotspot.Semantic proximity Read ↗

G to A polymorphism at amino acid codon 655 of the human erbB-2/HER2 gene.Semantic proximity Read ↗

A 40-nucleotide repeat polymorphism in the human dopamine transporter geneSemantic proximity Read ↗

Two novel mutations involved in hereditary tyrosinemia type I.Semantic proximity Read ↗

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