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Volumn 13, Issue 3, 2000, Pages 249-254
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Editorial: Is heterozygosity for a Wilson's disease gene defect an important underlying cause of infantile and childhood copper toxicosis syndromes?
a,b |
Author keywords
[No Author keywords available]
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Indexed keywords
COPPER;
EDITORIAL;
GENE MUTATION;
HETEROZYGOSITY;
HUMAN;
INTOXICATION;
LIVER CIRRHOSIS;
PRIORITY JOURNAL;
WILSON DISEASE;
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EID: 0033930725
PISSN: 0896548X
EISSN: None
Source Type: Journal
DOI: 10.1002/1520-670X(2000)13:3<249::AID-JTRA1>3.0.CO;2-L Document Type: Editorial |
Times cited : (8)
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References (20)
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