Aceruloplasminemia in an asymptomatic patient with a new mutation. Diagnosis and family genetic analysis
Author:
Publisher
Elsevier BV
Subject
Hepatology
Reference11 articles.
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2. A mutation in the ceruloplasmin gene associated with systemic hemosiderosis in humans;Yoshida;Nat Genet,1995
3. Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux;Harris;Proc Natl Acad Sci USA,1999
4. Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family;Morita;Ann Neurol,1995
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