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Volumn 13, Issue 3, 2000, Pages 249-254

Editorial: Is heterozygosity for a Wilson's disease gene defect an important underlying cause of infantile and childhood copper toxicosis syndromes?

Author keywords

[No Author keywords available]

Indexed keywords

COPPER;

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)

References (20)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.