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Volumn 1, Issue 10, 1996, Pages 453-459
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Primary hyperoxaluria type I: an inborn error of glyoxylate metabolism.
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Author keywords
[No Author keywords available]
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Indexed keywords
ALANINE GLYOXYLATE AMINOTRANSFERASE;
ALANINE-GLYOXYLATE TRANSAMINASE;
AMINOTRANSFERASE;
GLYOXYLIC ACID;
GLYOXYLIC ACID DERIVATIVE;
BIOLOGICAL MODEL;
GENETIC POLYMORPHISM;
GENETICS;
HUMAN;
HYPEROXALURIA;
LIVER TRANSPLANTATION;
METABOLISM;
PATHOPHYSIOLOGY;
REVIEW;
GLYOXYLATES;
HUMANS;
HYPEROXALURIA;
LIVER TRANSPLANTATION;
MODELS, BIOLOGICAL;
POLYMORPHISM, GENETIC;
TRANSAMINASES;
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EID: 0030601147
PISSN: 09492321
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
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Times cited : (2)
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References (39)
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