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Volumn 57, Issue 12, 2001, Pages 2205-2210

Cerebellar ataxia associated with heteroallelic ceruloplasmin gene mutation

Author keywords

[No Author keywords available]

Indexed keywords

CERULOPLASMIN;

EID: 0035956555     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.57.12.2205     Document Type: Article
Times cited : (66)

References (32)
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    • Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel
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    • Zhuchenko, O.1    Bailey, J.2    Bonnen, P.3
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    • 0031793132 scopus 로고    scopus 로고
    • The significance of haemochromatosis gene mutations in the general population: Implications for screening
    • (1998) Gut , vol.43 , pp. 830-836
    • Burt, M.J.1    George, P.M.2    Upton, J.D.3
  • 21
    • 0034891099 scopus 로고    scopus 로고
    • Increased oxysterols associated with iron accumulation in the brains and visceral organs of aceruloplasminemia patients
    • (2001) Q J Med , vol.94 , pp. 417-422
    • Miyajima, H.1    Adachi, J.2    Kohno, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.