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Association between heterozygous α1-antitrypsin deficiency and genetic hemochromatosis

✍ Scribed by Raimund Kaserbacher; Theresa Propst; Albert Propst; Ivo Graziadei; Gert Judmaier; Wolfgang Vogel

Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
153 KB
Volume
18
Category
Article
ISSN
0270-9139

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✦ Synopsis

Mieli-Vergani G. Value of urinary copper excretion after penicillamine challenge in the diagnosis of Wilson's disease. HEPATOLOGY

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