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Article

Novel AGXT gene mutation in a Sri Lankan family with primary Hyperoxaluria type 1.

Nephrology (Carlton, Vic.) - 1 Jan 2016

Sirisena Nirmala D, Tantrigoda Nethra Hidellage, Kariyawasam Kariyawasam Jayani C, Jayasekara Rohan W, Dissanayake Vajira H W

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Share to Consanguinity
Share to Hyperoxaluria, Primary
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 26693850
DOI: 10.1111/nep.12572

Genes

AGXT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Novel AGXT gene mutation in a Sri Lankan family with primary Hyperoxaluria type 1.PMID 26693850Read ↗

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Expanding the Genetic Spectrum of AGXT Gene Variants in Egyptian Patients with Primary Hyperoxaluria Type I.Semantic proximity Read ↗

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

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Selected AGXT gene mutations analysis provides a genetic diagnosis in 28% of Tunisian patients with primary hyperoxaluria.Semantic proximity Read ↗

A novel mutation in the AGXT gene causing primary hyperoxaluria type I: genotype-phenotype correlation.Semantic proximity Read ↗

Molecular analysis of the AGXT gene in patients suspected with hyperoxaluria type 1 and three novel mutations from Turkey.Semantic proximity Read ↗

[Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder].Semantic proximity Read ↗

Molecular analysis of the AGXT gene in Syrian patients suspected with primary hyperoxaluria type 1.Semantic proximity Read ↗

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