Structure of the Wilson disease copper transporter ATP7B | Science Advances
Full-length ATP7B reconstituted through protein trans-splicing corrects Wilson disease in mice: Molecular Therapy - Methods & Clinical Development
Overview of the human ATP7A and ATP7B ATPases. The proteins contain six... | Download Scientific Diagram
Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson disease | BMC Medical Genetics | Full Text
Domain composition of ATP7B and the distribution of the Wilson disease... | Download Scientific Diagram
Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson disease | BMC Medical Genetics | Full Text
ATP7B Gene - GeneCards | ATP7B Protein | ATP7B Antibody
Full-length ATP7B reconstituted through protein trans-splicing corrects Wilson disease in mice: Molecular Therapy - Methods & Clinical Development
The ATP7B Gene - ScienceDirect
Wilson disease protein - Wikipedia
Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their properties | Scientific Reports
ATP7B variant c.1934T > G p.Met645Arg causes Wilson disease by promoting exon 6 skipping | npj Genomic Medicine
Schematic representation of ATP7B mutations detected in the present... | Download Scientific Diagram
Mnemonics Worth Sharing - #Mnemonic #Pathology #Gastrointestinal Wilson disease (Hepatolenticular degeneration ) ATP7B gene chromosomal location. | Facebook
Production of Wilson Disease Model Rabbits with Homology-Directed Precision Point Mutations in the ATP7B Gene Using the CRISPR/Cas9 System | Scientific Reports
Figure 3.1 from The genetics of Wilson disease. | Semantic Scholar
Genetic variation spectrum in ATP7B gene identified in Latvian patients with Wilson disease - Zarina - 2017 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson disease | BMC Medical Genetics | Full Text
ATP7B Gene (ATPase Copper Transporting Beta) - StoryMD
Distinct phenotype of a Wilson disease mutation reveals a novel trafficking determinant in the copper transporter ATP7B | PNAS
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
Cellular Function of ATP7B (Wilson ATPase) - ScienceDirect
Whole‐exome sequencing identifies novel pathogenic variants across the ATP7B gene and some modifiers of Wilson's disease phenotype - Kluska - 2019 - Liver International - Wiley Online Library
Schematic presentation of ATP7B gene structure in DNA (a) and protein... | Download Scientific Diagram
Wilson disease protein - Wikipedia
