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Article

TaqI RFLP for the human fumarylacetoacetate hydrolase (FAH) gene.

Nucleic acids research - 25 Mar 1991

Demers S I, Phaneuf D, Tanguay R M

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 1674367
DOI: 10.1093/nar/19.6.1352-a
PMCID: PMC333878

Genes

FAH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

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Research trail→

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TaqI RFLP for the human fumarylacetoacetate hydrolase (FAH) gene.PMID 1674367Read ↗

The human fumarylacetoacetase gene: characterisation of restriction fragment length polymorphisms and identification of haplotypes in tyrosinemia type 1 and pseudodeficiency.Semantic proximity Read ↗

Six novel mutations in the fumarylacetoacetate hydrolase gene of patients with hereditary tyrosinemia type I.Semantic proximity Read ↗

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Mutations in the fumarylacetoacetate hydrolase gene causing hereditary tyrosinemia type I: overview.Semantic proximity Read ↗

Structural organization and analysis of the human fumarylacetoacetate hydrolase gene in tyrosinemia type I.Semantic proximity Read ↗

Two novel FAH gene mutations in a patient with hereditary tyrosinemia type I.Semantic proximity Read ↗

An improved method for genotyping of N-acetyltransferase polymorphism by polymerase chain reaction.Semantic proximity Read ↗

A novel polymorphic allele of human arylacetamide deacetylase leads to decreased enzyme activity.Semantic proximity Read ↗

Spectrum of mutations in the fumarylacetoacetate hydrolase gene of tyrosinemia type 1 patients in northwestern Europe and Mediterranean countries.Semantic proximity Read ↗

Compound mutations (R237X and L375P) in the fumarylacetoacetate hydrolase gene causing tyrosinemia type I in a Chinese patient.Semantic proximity Read ↗

Molecular Aspects of the FAH Mutations Involved in HT1 Disease.Semantic proximity Read ↗

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