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Volumn 45, Issue 5, 2000, Pages 275-279

Molecular analysis of Wilson disease in Taiwan: Identification of one novel mutation and evidence of haplotype-mutation association

Author keywords

ATP7B; Haplotype analysis; Mutation analysis; Short tandem repeat (STR) markers; Taiwanese; Wilson disease (WND)

Indexed keywords

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENETIC HETEROGENEITY; GENETIC POLYMORPHISM; HAPLOTYPE; HUMAN; MALE; MISSENSE MUTATION; PEDIGREE; TAIWAN; TANDEM REPEAT; WILSON DISEASE;

EID: 0033776322     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380070015     Document Type: Article
Times cited : (17)

References (19)
  • 5
    • 0000386450 scopus 로고
    • Disorders of copper transport
    • Scriver CR, Beaudet AL, Sly WS, Valle D (eds). The metabolic and molecular bases of inherited disease, 7th ed. McGraw-Hill, New York
    • (1995) , pp. 2211-2235
    • Danks, D.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.