Functional Synergism between the Most Common Polymorphism in Human Alanine:Glyoxylate Aminotransferase and Four of the Most Common Disease-causing Mutations-Reference-Cited by-同舟云学术

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Functional Synergism between the Most Common Polymorphism in Human Alanine:Glyoxylate Aminotransferase and Four of the Most Common Disease-causing Mutations

Published:2000-11 Issue:46 Volume:275 Page:36415-36422
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Lumb Michael J.,Danpure Christopher J.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference46 articles.

1. Pediatric Nephrology;Barratt,1999

2. Kidney Stones: Medical and Surgical Management;Danpure,1996

3. The Metabolic and Molecular Bases of Inherited Disease;Danpure,1995

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

5. STRATEGIES FOR THE PRENATAL DIAGNOSIS OF PRIMARY HYPEROXALURIA TYPE 1

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