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Volumn 5, Issue 3, 2013, Pages 156-159

Genetically confirmed wilson disease in a 9-month old boy with elevations of aminotransferases

Author keywords

Early diagnosis; Hepatolenticular degeneration; Molecular genetics; Mutation; Wilson disease

Indexed keywords


EID: 84879190000     PISSN: None     EISSN: 19485182     Source Type: Journal    
DOI: 10.4254/wjh.v5.i3.156     Document Type: Article
Times cited : (42)

References (14)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.