Homo sapiens alanine-glyoxylate aminotransferase homolog (TLH6) mRNA, - Nucleotide

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Expanding the Genetic Spectrum of AGXT Gene Variants in Egyptian Patients with Primary Hyperoxaluria Type I. [Genet Test Mol Biomarkers. 2024]
Expanding the Genetic Spectrum of AGXT Gene Variants in Egyptian Patients with Primary Hyperoxaluria Type I.
Naguib S, Mansour LA, Soliman NA, El-Hanafy HM, Fahmy YA, Elmonem MA, Halim RMA. Genet Test Mol Biomarkers. 2024 Apr; 28(4):151-158.
Insights into the pathogenesis of primary hyperoxaluria type I from the structural dynamics of alanine:glyoxylate aminotransferase variants. [FEBS Lett. 2024]
Insights into the pathogenesis of primary hyperoxaluria type I from the structural dynamics of alanine:glyoxylate aminotransferase variants.
Vankova P, Pacheco-Garcia JL, Loginov DS, Gómez-Mulas A, Kádek A, Martín-Garcia JM, Salido E, Man P, Pey AL. FEBS Lett. 2024 Feb; 598(4):485-499. Epub 2024 Jan 19.
Case series and literature review of primary hyperoxaluria type 1 in Chinese patients. [Urolithiasis. 2023]
Case series and literature review of primary hyperoxaluria type 1 in Chinese patients.
Wu J, Song J, He Y, Zhong C, Yang Q, Li Q, Wang M. Urolithiasis. 2023 Oct 24; 51(1):123. Epub 2023 Oct 24.

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Nucleotide