Wilson disease protein - Wikipedia
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
Full-length ATP7B reconstituted through protein trans-splicing corrects Wilson disease in mice: Molecular Therapy - Methods & Clinical Development
Domain composition of ATP7B and the distribution of the Wilson disease... | Download Scientific Diagram
Mnemonics Worth Sharing - #Mnemonic #Pathology #Gastrointestinal Wilson disease (Hepatolenticular degeneration ) ATP7B gene chromosomal location. | Facebook
Full-length ATP7B reconstituted through protein trans-splicing corrects Wilson disease in mice: Molecular Therapy - Methods & Clinical Development
Wilson Disease Protein ATP7B Utilizes Lysosomal Exocytosis to Maintain Copper Homeostasis: Developmental Cell
Solution Structures of the Actuator Domain of ATP7A and ATP7B, the Menkes and Wilson Disease Proteins | Biochemistry
Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson disease | BMC Medical Genetics | Full Text
ATP7B variant c.1934T > G p.Met645Arg causes Wilson disease by promoting exon 6 skipping | npj Genomic Medicine
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
Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their properties | Scientific Reports
Spectrum and Classification of ATP7B Variants in a Large Cohort of Chinese Patients with Wilson's Disease Guides Genetic Diagnosis
Cellular Function of ATP7B (Wilson ATPase) - ScienceDirect
Wilson disease protein - Wikipedia
Schematic representation of ATP7B mutations detected in the present... | Download Scientific Diagram
Functional analysis and drug response to zinc and D-penicillamine in stable ATP7B mutant hepatic cell lines
The conformation of the ATP7B protein and marking of 2 prominent... | Download Scientific Diagram
Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson disease | BMC Medical Genetics | Full Text
Function and Regulation of Human Copper-Transporting ATPases | Physiological Reviews
Vivet Therapeutics' Gene Therapy for Wilson's Disease gets Orphan Status
