Author:
Knight John,Holmes Ross P.,Milliner Dawn S.,Monico Carla G.,Cramer Scott D.
Publisher
Oxford University Press (OUP)
Subject
Transplantation,Nephrology
Reference15 articles.
1. Danpure CJ. Primary hyperoxaluria. In: Scriver CR, Beaudet AL, Sly WS et al. (eds). The Metabolic and Molecular Bases of Inherited Disease. McGraw-Hill, New York: 2001; 3323–3367
2. Cramer SD, Ferree PM, Lin K, Milliner DS, Holmes RP. The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patients with Primary Hyperoxaluria Type II. Hum Mol Genet1999; 11: 2063–2069
3. Williams HE, Smith LHJ. L-glyceric aciduria. A new genetic variant of primary hyperoxaluria. New Engl J Med1968; 278: 233–239
4. Cregeen DP, Williams EL, Hulton S, Rumsby G. Molecular analysis of the glyoxylate reductase (GRHPR) gene and description of mutations underlying primary hyperoxaluria type 2. Hum Mutat2003; 22: 497–505
5. Webster KE, Ferree PM, Holmes RP, Cramer SD. Identification of missense, nonsense, and deletion mutations in the GRHPR gene in patients with primary hyperoxaluria type II (PH2). Human Gen2000; 107: 176–185
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