메뉴 건너뛰기




Volumn 43, Issue 4, 2000, Pages 925-929

Localization of a gene for familial juvenile hyperuricemic nephropathy causing underexcretion-type gout to 16p12 by genome-wide linkage analysis of a large family

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

EID: 0033850904     PISSN: 00043591     EISSN: None     Source Type: Journal    
DOI: 10.1002/1529-0131(200004)43:4<925::AID-ANR26>3.0.CO;2-B     Document Type: Article
Times cited : (63)

References (15)
  • 1
    • 0001530462 scopus 로고
    • Hyperuricemia and gout
    • Scriver CR, Beaudet AL, Sly WS, Valle D, editors. Metabolic and molecular basis of inherited disease. New York: McGraw-Hill
    • (1995) , pp. 1655-1678
    • Becker, M.A.1    Roessler, B.J.2
  • 9
    • 0002939438 scopus 로고    scopus 로고
    • Inherited disorders of purine metabolism and transport
    • Davison AM, Cameron JS, Grunfield J-P, Kerr DNS, Ritz E, Wincarls CG, editors. Oxford textbook of clinical nephrology. Oxford: University Press
    • (1997) , pp. 2469-2482
    • Cameron, J.S.1    Moro, F.2    McBride, M.B.3    Simmonds, H.A.4
  • 13
    • 0001127049 scopus 로고
    • Hypoxanthine-guanine phosphoribosyl-transferase deficiency: Lesch-Nyhan syndrome and gout
    • Scriver CR, Beaudet AL, Sly WS, Valle D, editors. Metabolic and molecular basis of inherited disease. New York: McGraw-Hill
    • (1995) , pp. 1679-1706
    • Rossiter, B.J.F.1    Caskey, C.T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.