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References
These sources were used to develop the Genetics Home Reference
gene summary
on the AGXT gene.
Coulter-Mackie MB, Applegarth D, Toone JR, Henderson H. The major allele of the alanine:glyoxylate aminotransferase gene: seven novel mutations causing primary hyperoxaluria type 1. Mol Genet Metab. 2004 May;82(1):64-8.
PubMed citation
Coulter-Mackie MB. Preliminary Evidence for Ethnic Differences in Primary Hyperoxaluria Type 1 Genotype. Am J Nephrol. 2005 Jun 15;25(3):264-268 [Epub ahead of print].
PubMed citation
Danpure CJ. Molecular aetiology of primary hyperoxaluria type 1. Nephron Exp Nephrol. 2004;98(2):e39-44.
PubMed citation
Danpure CJ. Primary hyperoxaluria type 1: AGT mistargeting highlights the fundamental differences between the peroxisomal and mitochondrial protein import pathways. Biochim Biophys Acta. 2006 Dec;1763(12):1776-84. Epub 2006 Aug 24. Review.
PubMed citation
Gene Review: Hyperoxaluria, Primary, Type
1
Pirulli D, Marangella M, Amoroso A. Primary hyperoxaluria: genotype-phenotype correlation. J Nephrol. 2003 Mar-Apr;16(2):297-309. Review.
PubMed citation
Yuen YP, Lai CK, Tong GM, Wong PN, Wong FK, Mak SK, Lo KY, Wong AK, Tong SF, Chan YW, Lam CW. Novel mutations of the AGXT gene causing primary hyperoxaluria type 1. J Nephrol. 2004 May-Jun;17(3):436-40.
PubMed citation
Reviewed: January 2008
Published: February 6, 2009