Primary and secondary hyperoxaluria: Understanding the enigma

doi:10.5527/wjn.v4.i2.235

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World Journal of Nephrology

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2220-6124

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Nephrol. May 6, 2015; 4(2): 235-244
Published online May 6, 2015. doi: 10.5527/wjn.v4.i2.235

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Figure 1 Pathway of oxalate synthesis and enzymatic defects in PH. A: PH1, alanine glyoxalate aminotransferase; B: PH 2, glycolate reductase hydroxy pyruvate reductase; C: PH 3, 4-hydroxy 2-ketoglutarate aldolase; D: Lactate dehydrogenase.

Citation: Bhasin B, Ürekli HM, Atta MG. Primary and secondary hyperoxaluria: Understanding the enigma. World J Nephrol 2015; 4(2): 235-244
URL: https://www.wjgnet.com/2220-6124/full/v4/i2/235.htm
DOI: https://dx.doi.org/10.5527/wjn.v4.i2.235