Indian childhood cirrhosis and tyrolean childhood cirrhosis: Disorders of a copper transport gene?

Advances in Experimental Medicine and Biology

Volumn 448, Issue , 1999, Pages 127-137

  Tanner, M S ^a  

^a UNIVERSITY OF SHEFFIELD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CERULOPLASMIN; CHAPERONE; COPPER; GENE PRODUCT; METALLOTHIONEIN; UNCLASSIFIED DRUG; WILSON DISEASE PROTEIN;

CHILDHOOD DISEASE; CONFERENCE PAPER; COPPER METABOLISM; DIFFERENTIAL DIAGNOSIS; ENVIRONMENTAL FACTOR; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; HEMOCHROMATOSIS; HUMAN; INDIAN CHILDHOOD CIRRHOSIS; LIVER CIRRHOSIS; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; TYROLEAN CHILDHOOD CIRRHOSIS; WILSON DISEASE;

EID: 0033278274     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-4615-4859-1_11     Document Type: Conference Paper

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