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Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease
5个月前
已完结
The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene
5个月前
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Molecular characterization of Wilson disease in the Sardinian population?Evidence of a founder effect
5个月前
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Mapping, cloning and genetic characterization of the region containing the Wilson disease gene
5个月前
已完结
Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype–phenotype correlation in Indian patients
5个月前
已完结
Mutation analysis of 73 southern Chinese Wilson's disease patients: identification of 10 novel mutations and its clinical correlation
5个月前
已完结
Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype-phenotype correlation in Indian patients
5个月前
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