Enxymological characterization of a putative canine analogue of primary hyperoxaluria type 1-Reference-Cited by-同舟云学术

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Enxymological characterization of a putative canine analogue of primary hyperoxaluria type 1

Published:1991-02 Issue:2 Volume:1096 Page:134-138
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Danpure Christopher J.,Jennings Patricia R.,Johan H. Jansen

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference14 articles.

1. The Metabolic Basis of Inherited Disease;Williams,1983

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

3. Further studies on the activity and subcellular distribution of alanine: Glyoxylate aminotransferase in the livers of patients with primary hyperoxaluria type 1

4. L-Glyceric Aciduria

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

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5. Hyperoxaluria, hyperglycoluria and renal oxalosis in Gilbert's potoroos (Potorous gilbertii );Australian Veterinary Journal;2017-06-26

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