Genetic analysis: A diagnostic tool for primary hyperoxaluria type 1 (multiple letter) [3]

Pediatric Nephrology

Volumn 18, Issue 5, 2003, Pages 482-483

  von Schnakenburg, Christian ^a   Rumsby, Gill ^b   Hoppe, Bernd ^c   Latta, Kay ^d   Kemper, Markus ^e   Rinat, Choni ^f   Milosevic, Danko ^g   Frishberg, Yaacov ^f  

^a UNIVERSITY OF FREIBURG   (Germany)

^b UNIVERSITY COLLEGE LONDON HOSPITALS   (United Kingdom)

^c Division of Pediatric Nephrology   (Germany)

^d HANNOVER MEDICAL SCHOOL   (Germany)

^e UNIVERSITY CHILDREN S HOSPITAL   (Switzerland)

^f SHAARE ZEDEK MEDICAL CENTER   (Israel)

^g Croatia   (Croatia)

Author keywords

Diagnosis; Genetic analysis; Primary hyperoxaluria type 1

Indexed keywords

ALANINE GLYOXYLATE AMINOTRANSFERASE; LIVER ENZYME;

DIAGNOSTIC VALUE; GENETIC ANALYSIS; GENETIC CODE; GENETIC SCREENING; HUMAN; KIDNEY TRANSPLANTATION; LETTER; LINKAGE ANALYSIS; LIVER TRANSPLANTATION; MUTATIONAL ANALYSIS; OXALOSIS 1; PRIORITY JOURNAL; SENSITIVITY ANALYSIS; SEQUENCE ANALYSIS;

EID: 0038419659     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-003-1107-3     Document Type: Letter

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