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Volumn 24, Issue 3, 2009, Pages 463-468

Heterozygous carriers for Wilson's disease-magnetic spectroscopy changes in the brain

Author keywords

Heterozygous carriers; Magnetic resonance spectroscopy; Wilson disease

Indexed keywords

CERULOPLASMIN; CHOLINE; COPPER; CREATINE; GLUTAMIC ACID; LIPID; N ACETYLASPARTIC ACID;

EID: 70350031071     PISSN: 08857490     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11011-009-9145-6     Document Type: Article
Times cited : (18)

References (13)
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    • Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease
    • G Gromadzka H Schmidt J Genschel B Bochow M Rodo B Tarnacka T Litwin G Chabik A Członkowska 2006 Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease Clin Genet 68 524 532
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    • Gromadzka, G.1    Schmidt, H.2    Genschel, J.3    Bochow, B.4    Rodo, M.5    Tarnacka, B.6    Litwin, T.7    Chabik, G.8    Członkowska, A.9
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    • S Johnson 2001 Is Parkinson's disease the heterozygote form of Wilson's disease: PD=1/2 WD? Med Hypotheses 56 171 173 10.1054/mehy.2000.1134 1:STN:280:DC%2BD3Mzntlemuw%3D%3D 11425282 (Pubitemid 32202623)
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    • Trace amounts of copper in water induce β-amyloid plaques and learning deficits in a rabbit model of Alzheimer's disease
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.