Ethnic differences inGRHPRmutations in patients with primary hyperoxaluria type 2-Reference-Cited by-同舟云学术

Ethnic differences inGRHPRmutations in patients with primary hyperoxaluria type 2

Published:2013-11-05 Issue:4 Volume:86 Page:342-348
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Takayama T.¹,Takaoka N.¹,Nagata M.¹,Johnin K.²,Okada Y.²,Tanaka S.³,Kawamura M.⁴,Inokuchi T.⁵,Ohse M.⁶,Kuhara T.⁶⁷,Tanioka F.⁸,Yamada H.⁹,Sugimura H.⁹,Ozono S.¹

Affiliation:

1. Department of Urology; Hamamatsu University School of Medicine; Hamamatsu Japan

2. Department of Urology; Shiga University of Medical Science; Otsu Japan

3. Department of Pediatrics; Kurume University Medical Center; Kurume Japan

4. Kawamura Children's Clinic; Nagoya Japan

5. Research Institute of Medical Mass Spectrometry; Kurume University School of Medicine; Kurume Japan

6. Japan Clinical Metabolomics Institute; Kahoku Japan

7. Division of Human Genetics, Medical Research Institute; Kanazawa Medical University; Uchinada Japan

8. Division of Pathology; Iwata City Hospital; Iwata Japan

9. Department of Tumor Pathology; Hamamatsu University School of Medicine; Hamamatsu Japan

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference18 articles.

1. Primary Hyperoxaluria

2. Glyoxylate reductase activity in blood mononuclear cells and the diagnosis of primary hyperoxaluria type 2;Knight;Nephrol Dial Transplant,2006

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

4. Molecular analysis of the glyoxylate reductase (GRHPR) gene and description of mutations underlying primary hyperoxaluria type 2;Cregeen;Hum Mutat,2003

5. Primary hyperoxaluria type 2 in children;Johnson;Pediatr Nephrol,2002

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