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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. doi: 10.1016/j.ymgme.2004.02.001.
Mol Genet Metab. 2004.
PMID: 15110324
Primary Hyperoxaluria Type 1.
Milliner DS, Harris PC, Sas DJ, Cogal AG, Lieske JC.
Milliner DS, et al.
2002 Jun 19 [updated 2022 Feb 10]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
2002 Jun 19 [updated 2022 Feb 10]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID: 20301460
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