'C 3207c' diaporamas de présentation

A review of the Wilson disease service over the past 15 years

A review of the Wilson disease service over the past 15 years. Miranda Durkie Sheffield Diagnostic Genetics Service miranda.durkie@sch.nhs.uk. Introduction. Wilson disease (WD; OMIM#277900) is an autosomal recessive disorder of copper metabolism Hepatic and/or neurological presentation

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