Analysis of Wilson disease mutations in copper binding domain of ATP7B gene
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DOI: 10.1371/journal.pone.0269833
Abstract: Wilson’s disease (WD) is an autosomal recessive disorder, resulting from variations in ATP7B gene. Clinical heterogeneity, including neuropsychiatric and hepatic manifestations over a large range of age groups make diagnosis difficult. Most of WD patients… read more here.
Keywords: disease; atp7b gene; analysis wilson; wilson disease ... See more keywords