Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant?

American Journal of Human Genetics

Volumn 63, Issue 6, 1998, Pages 1663-1674

  Forbes, John R ^a   Cox, Diane W ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; COPPER;

ARTICLE; CONTROLLED STUDY; COPPER METABOLISM; GENETIC LINKAGE; HUMAN; MISSENSE MUTATION; NONHUMAN; PRIORITY JOURNAL; WILSON DISEASE;

EID: 0032471911     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302163     Document Type: Article

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