Primary hyperoxaluria type 1: Diagnostic relevance of mutations and polymorphisms in the alanine:glyoxylate aminotransferase gene (AGXT)

Journal of Inherited Metabolic Disease

Volumn 20, Issue 5, 1997, Pages 689-696

  Tarn, A C ^a   Von Schnakenburg, C ^a   Rumsby, G ^a  

^a UNIVERSITY COLLEGE LONDON HOSPITALS   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE GLYOXYLATE AMINOTRANSFERASE;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; DNA POLYMORPHISM; FEMALE; GENE INSERTION; GENE MUTATION; GENETIC HETEROGENEITY; HUMAN; INFANT; INTRON; MAJOR CLINICAL STUDY; MALE; NEWBORN; OXALOSIS 1; POINT MUTATION; PRESCHOOL CHILD; SCHOOL CHILD; TANDEM REPEAT;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; HYPEROXALURIA; INFANT; MALE; MIDDLE AGED; MUTATION; POLYMORPHISM, GENETIC; TRANSAMINASES;

EID: 0030846656     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/a:1005326510239     Document Type: Article

References (24)

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