Late Diagnosis of Primary Hyperoxaluria Type 2 in the Adult: Effect of a Novel Mutation in GRHPR Gene on Enzymatic Activity and Molecular Modeling-Reference-Cited by-同舟云学术

Late Diagnosis of Primary Hyperoxaluria Type 2 in the Adult: Effect of a Novel Mutation in GRHPR Gene on Enzymatic Activity and Molecular Modeling

Published:2009-05 Issue:5 Volume:181 Page:2146-2151
ISSN:0022-5347
Container-title:Journal of Urology
language:en
Short-container-title:Journal of Urology

Author:

Levin-Iaina Nomy¹,Dinour Dganit¹,Romero Lina²,Ron Rotem¹,Brady R. Leo³,Cramer Scott D.²,Holtzman Eli J.¹

Affiliation:

1. Nephrology and Hypertension Institute, Department of Medicine, Tel Aviv University and Sackler School of Medicine, Chaim Sheba Medical Center, Tel Hashomer, Tel Aviv, Israel

2. Department of Cancer Biology, Wake Forest University School of Medicine, Winston-Salem, North Carolina

3. Department of Biochemistry, University of Bristol, Bristol, United Kingdom

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Urology

Reference13 articles.

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2. Time trends in reported prevalence of kidney stones in the US: 1976-1994;Stamatelou;Kidney Int,2003

3. Primary hyperoxaluria;Danpure,2001

4. The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patients with primary hyperoxaluria type 2;Cramer;Hum Mol Genet,1999

5. Hyperoxaluria in L-glyceric aciduria: possible pathogenic mechanism;Williams;Science,1971

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