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Article

Possible association of catecholamine turnover with the polymorphic (TCAT)n repeat in the first intron of the human tyrosine hydroxylase gene.

Life sciences - 1 Jan 1997

Wei J, Ramchand C N, Hemmings G P

Abstract excerpt

Five allelic fragments were typed by a PCR-based process with a pair of primers specific for the polymorphic sequence due to (TCAT)n tetranucleotide repeat, a microsatellite repeat, in the first intron of the human tyrosine hydroxylase gene, i.e. A1, A2, A3, A4 and A5. Comparisons of some neurochemical parameters of the catecholamine pathway were then made between the unrelated individuals genotypically...

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Share to Catecholamines
Share to Genotype
Share to Homozygote

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

Share to Introns

Share to Polymorphism, Genetic

Share to Repetitive Sequences, Nucleic Acid

Share to RNA, Messenger

Share to Tyrosine 3-Monooxygenase

Source

Identifiers

PMID: 9335223
DOI: 10.1016/s0024-3205(97)00679-6

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.

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