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Wilson Disease Protein ATP7B Utilizes Lysosomal Exocytosis to Maintain Copper Homeostasis: Developmental Cell
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Solution Structures of the Actuator Domain of ATP7A and ATP7B, the Menkes and Wilson Disease Proteins | Biochemistry
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ATP7B variant c.1934T > G p.Met645Arg causes Wilson disease by promoting exon 6 skipping | npj Genomic Medicine
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Full-length ATP7B reconstituted through protein trans-splicing corrects Wilson disease in mice: Molecular Therapy - Methods & Clinical Development
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Schematic representation of ATP7B mutations detected in the present... | Download Scientific Diagram
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Wilson disease missense mutations in ATP7B affect metal-binding domain structural dynamics | SpringerLink
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Spectrum and Classification of ATP7B Variants in a Large Cohort of Chinese Patients with Wilson's Disease Guides Genetic Diagnosis
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Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their properties | Scientific Reports
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Genes | Free Full-Text | Prevalent Pathogenic Variants of ATP7B in Chinese Patients with Wilson's Disease: Geographical Distribution and Founder Effect
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Non-ceruloplasmin bound copper and ATP7B gene variants in Alzheimer's disease - Metallomics (RSC Publishing) DOI:10.1039/C6MT00101G
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International Wilson Disease Mutation Database-国际肝豆状核变性基因突变数据库--The pathogenisis of Wilson's disease
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