Family Study of 2,8-Dihydroxyadenine Stone Formation: Report of Two Cases of a Compound Heterozygote for Adenine Phosphoribosyltransferase Deficiency (APRT*J/APRT*Q0)

International Journal of Urology

Volumn 4, Issue 3, 1997, Pages 304-306

  Suzuki, Koji ^a   Kobayashi, Shigeyuki ^b   Kawamura, Kenji ^b   Kuhara, Tomiko ^a   Tsugawa, Ryuzo ^a  

^a KANAZAWA MEDICAL UNIVERSITY   (Japan)

^b Asanogawa General Hospital   (Japan)

Author keywords

2,8 dihydroxyadenine stone; APRT deficiency; Compound heterozygote (APRT*J APRT*Q0)

Indexed keywords

2,8 DIHYDROXYADENINE; 2,8-DIHYDROXYADENINE; ADENINE; ADENINE PHOSPHORIBOSYLTRANSFERASE; DRUG DERIVATIVE;

ADULT; ARTICLE; CASE REPORT; CHEMISTRY; ENZYMOLOGY; FAMILY HEALTH; FEMALE; GENETICS; GENOTYPE; HUMAN; MALE; METABOLISM; NEPHROLITHIASIS; PEDIGREE; URINE;

ADENINE; ADENINE PHOSPHORIBOSYLTRANSFERASE; ADULT; FAMILY HEALTH; FEMALE; GENOTYPE; HUMANS; KIDNEY CALCULI; MALE; PEDIGREE; URINE;

EID: 0031132116     PISSN: 09198172     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1442-2042.1997.tb00195.x     Document Type: Article

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