The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3-Reference-Cited by-同舟云学术

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The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3

Published:2012-03-05 Issue:8 Volume:27 Page:3191-3195
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrology Dialysis Transplantation

Author:

Williams E. L.,Bockenhauer D.,van't Hoff W. G.,Johri N.,Laing C.,Sinha M. D.,Unwin R.,Viljoen A.,Rumsby G.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/27/8/3191/7638141/gfs039.pdf

Reference16 articles.

1. Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

2. Hepatic d-glycerate dehydrogenase and glyoxylate reductase deficiency in primary hyperoxaluria type 2

3. Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: A novel type of primary hyperoxaluria

4. Hyperoxaluria and Urolithiasis in Young Children: An Atypical Presentation

5. Mutations in DHDPSL Are Responsible For Primary Hyperoxaluria Type III

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