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Article

Dinucleotide repeat polymorphism at the locus for human ferrochelatase (FECH).

Human molecular genetics - 1 Jun 1993

Whitcombe D M, Cox T M

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Topics

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Share to Chromosomes, Human, Pair 18
Share to Ferrochelatase
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymerase Chain Reaction

Share to Repetitive Sequences, Nucleic Acid

Source

Identifiers

PMID: 8353511
DOI: 10.1093/hmg/2.6.826

Genes

FECH

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Dinucleotide repeat polymorphism at the locus for human ferrochelatase (FECH).PMID 8353511Read ↗

A novel large deletion and three polymorphisms in the FECH gene associated with erythropoietic protoporphyria.Semantic proximity Read ↗

Variations in the length of poly-C and poly-T tracts in intron 3 of the human ferrochelatase gene.Semantic proximity Read ↗

Digital PCR (dPCR) analysis reveals that the homozygous c.315-48T>C variant in the FECH gene might cause erythropoietic protoporphyria (EPP).Semantic proximity Read ↗

A homozygous mutation in the ferrochelatase gene underlies erythropoietic protoporphyria associated with palmar keratoderma.Semantic proximity Read ↗

Dinucleotide repeat polymorphism at the human CD59 locus.Semantic proximity Read ↗

Dinucleotide repeat polymorphism at the FTHPI locus of chromosome 6.Semantic proximity Read ↗

Dinucleotide repeat polymorphism in the human estrogen receptor (ESR) gene.Semantic proximity Read ↗

Hypermethylation of the wild-type ferrochelatase allele is closely associated with severe liver complication in a family with erythropoietic protoporphyria.Semantic proximity Read ↗

Four novel mutations in the ferrochelatase gene among erythropoietic protoporphyria patients.Semantic proximity Read ↗

Tetranucleotide repeat polymorphism at the human dihydrofolate reductase psi-2 pseudogene (DHFRP2).Semantic proximity Read ↗

A 10376 bp deletion of FECH gene responsible for erythropoietic protoporphyria.Semantic proximity Read ↗

A bi-allelic tetranucleotide repeat in the promoter of the human inducible nitric oxide synthase gene.Semantic proximity Read ↗

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