Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I.

Source:http://linkedlifedata.com/resource/pubmed/id/20133649

Proc. Natl. Acad. Sci. U.S.A. 2010 Feb 16 107 7 2896-901

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PMID
20133649