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Article

Gene symbol: AGXT. Disease: primary hyperoxaluria type I.

Human genetics - 1 May 1999

Amoroso A, Pirulli D, Puzzer D, Ferri L, Crovella S, Ferrettini C, Marangella M, Mazzola G, Florian F

Abstract excerpt

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Topics

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Share to Amino Acid Substitution
Share to Base Sequence
Share to DNA Transposable Elements
Share to AGXT gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hyperoxaluria, Primary

Share to Mutation

Share to Mutation, Missense

Share to Sequence Deletion

Source

Identifiers

PMID: 10394939
DOI: 10.1007/s004390050984

Genes

AGXT

Provenance

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Related research

Semantic proximity does not establish scientific evidence.

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Molecular Analysis of the AGXT Gene Detected a Missense and Pathogenic Variant Associated with Primary Hyperoxaluria Type 1; a Case StudySemantic proximity Read ↗

[From gene to disease; primary hyperoxaluria type I caused by mutations in the AGXT gene].Semantic proximity Read ↗

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