MOLECULAR DIAGNOSIS OF PRESYMPTOMATIC Wilson's Disease

Abstract

Wilson's disease (WND) is an autosomal recessive disorder of copper metabolism, The metabolic defect is still unknown, but the locus ol the disease has been mapped to chromosome 13q14-q21. Using polymorphic DNA markers in affected families, we are now able to recognize WND before the onset of clinical manifestations.PATIENTS AND METHODS 121 subjects have… (More)
DOI: 10.1203/00006450-199402000-00074

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