Molecular analysis of 53 Chinese families with Wilson's disease: Six novel mutations identified
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DOI: 10.1002/mgg3.1735
Abstract: Wilson's disease (WD) is a rare autosomal recessive inherited disorder that is induced by defects of the ATP7B gene and characterized by damage to the liver and nervous system caused by aberrant copper metabolism. The… read more here.
Keywords: families wilson; molecular analysis; analysis chinese; disease ... See more keywords