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Volumn 41, Issue 3, 2006, Pages 361-364

Poor cognitive development and abdominal pain: Wilson's disease

Author keywords

Dysphasia; Learning disabilities; Wilson's disease

Indexed keywords

ALANINE AMINOTRANSFERASE; CERULOPLASMIN; COPPER; PENICILLAMINE; WATER;

EID: 33644600458     PISSN: 00365521     EISSN: None     Source Type: Journal    
DOI: 10.1080/00365520510023431     Document Type: Article
Times cited : (8)

References (16)
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  • 4
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    • The Wilson's disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene
    • Bull PC, Thomas GR, Rommens JM, Forbes JR, Cox DW. The Wilson's disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nat Genet 1993; 5:327-37.
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  • 5
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    • The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
    • Tanzi RE, Petrukhin K, Chernov I, Pellequer JL, Wasco W, Ross B, et al. The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene. Nat Genet 1993;5:44-50.
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    • Tanzi, R.E.1    Petrukhin, K.2    Chernov, I.3    Pellequer, J.L.4    Wasco, W.5    Ross, B.6
  • 6
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    • Intracellular distribution of the Wilson's disease gene product (ATPase/B) after in vitro and in vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson's disease
    • Nagano K, Nakamura K, Urakami KI, Umeyama K, Uchiyama H, et al. Intracellular distribution of the Wilson's disease gene product (ATPase/B) after in vitro and in vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson's disease. Hepatology 1998;27:799-807.
    • (1998) Hepatology , vol.27 , pp. 799-807
    • Nagano, K.1    Nakamura, K.2    Urakami, K.I.3    Umeyama, K.4    Uchiyama, H.5
  • 7
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    • Oxidative-phosphorylation defects in liver of patients with Wilson's disease
    • Gu M, Cooper JM, Butler P, Walker AP, Mistry PK, Dooley JS, et al. Oxidative-phosphorylation defects in liver of patients with Wilson's disease. Lancet 2000;356:469-74.
    • (2000) Lancet , vol.356 , pp. 469-474
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  • 12
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    • Determination of the frequencies of the allelic variants of the Wilson disease gene (ATP7B) in pooled DNA samples
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    • (2000) Eur J Hum Genet , vol.8 , pp. 933-938
    • Olsson, C.1    Waldenstrom, E.2    Westermark, K.3    Landegre, U.4    Syvanen, A.C.5
  • 13
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    • Rapid detection of mutations in Wilson disease gene ATP7B by DNA strip technology
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    • Disorders of copper metabolism
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  • 16
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    • Treatment of Wilson's disease with zinc XVI: Treatment during the pediatric years
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    • Brewer, G.J.1    Dick, R.D.2    Johnson, V.D.3    Fink, J.K.4    Kluin, K.J.5    Daniels, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.