Lesch-Nyhan syndrome: Clinical diagnosis and confirmation by biochemical and genetic methods [1]

Pediatric Nephrology

Volumn 11, Issue 1, 1997, Pages 124-125

  Erbhard, U ^a   Herkenrath, P ^a   Benz Bohm, G ^a   Querfeld, U ^a  

^a UNIVERSITY HOSPITAL OF COLOGNE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE;

BIOCHEMISTRY; CASE REPORT; CHROMOSOME XQ; CLINICAL FEATURE; ECHOGRAPHY; ENZYME ACTIVITY; GENE LOCATION; GENETIC ANALYSIS; HUMAN; INFANT; LESCH NYHAN SYNDROME; LETTER; MALE; PRIORITY JOURNAL;

FIBROBLASTS; HUMANS; INFANT; KIDNEY; LESCH-NYHAN SYNDROME; MALE;

EID: 0031023554     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (10)