The Wilson disease gene is a putative copper transporting P-type ATPase similar to the menkes gene

Nature Genetics

Volumn 5, Issue 4, 1993, Pages 327-337

  Bull, Peter C ^a   Thomas, Gordon R ^a,b   Rommens, Johanna M ^a,b   Forbes, John R ^a   Cox, Diane Wilson ^a,b  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE;

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 13Q; CONTROLLED STUDY; COPPER METABOLISM; DNA SEQUENCE; GENE ISOLATION; GENE MUTATION; GENE REARRANGEMENT; HAMSTER; HUMAN; MENKES SYNDROME; NONHUMAN; SEQUENCE HOMOLOGY; WILSON DISEASE;

ADENOSINETRIPHOSPHATASE; AMINO ACID SEQUENCE; BASE SEQUENCE; BLOTTING, NORTHERN; CELL LINE; CHROMOSOMES, HUMAN, PAIR 13; COPPER; GENE EXPRESSION; HEPATOLENTICULAR DEGENERATION; HUMAN; MENKES KINKY HAIR SYNDROME; MOLECULAR SEQUENCE DATA; MUTATION; SEQUENCE ANALYSIS, DNA; SUPPORT, NON-U.S. GOV'T;

CRICETINAE; PROKARYOTA;

EID: 0027452091     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng1293-327     Document Type: Article

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