Wilson disease missense mutations in ATP7B affect metal-binding domain structural dynamics | SpringerLink
Genetic variation spectrum in ATP7B gene identified in Latvian patients with Wilson disease - Zarina - 2017 - Molecular Genetics & Genomic Medicine - Wiley Online Library
The genetics of Wilson disease. - Abstract - Europe PMC
Full-length ATP7B reconstituted through protein trans-splicing corrects Wilson disease in mice: Molecular Therapy - Methods & Clinical Development
Schematic representation of ATP7B mutations detected in the present... | Download Scientific Diagram
Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson disease | BMC Medical Genetics | Full Text
Distribution of mutations in the ATP7B gene in patients with Wilson... | Download Scientific Diagram
Wilson Disease Protein ATP7B Utilizes Lysosomal Exocytosis to Maintain Copper Homeostasis: Developmental Cell
Cells | Free Full-Text | Human Embryonic Stem Cell-Derived Wilson's Disease Model for Screening Drug Efficacy
Non-ceruloplasmin bound copper and ATP7B gene variants in Alzheimer's disease - Metallomics (RSC Publishing) DOI:10.1039/C6MT00101G
Progress toward improved Wilson's disease drug | Cold Spring Harbor Laboratory
Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson disease | BMC Medical Genetics | Full Text
Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their properties | Scientific Reports
Functional analysis and drug response to zinc and D-penicillamine in stable ATP7B mutant hepatic cell lines
What is ATP7B Gene Wilson disease NGS Genetic DNA Test ?
Production of Wilson Disease Model Rabbits with Homology-Directed Precision Point Mutations in the ATP7B Gene Using the CRISPR/Cas9 System | Scientific Reports
Mutation spectrum of ATP7B gene in pediatric patients with Wilson disease in Vietnam - ScienceDirect
The ATP7B Gene - ScienceDirect
Solution Structures of the Actuator Domain of ATP7A and ATP7B, the Menkes and Wilson Disease Proteins | Biochemistry
Distinct phenotype of a Wilson disease mutation reveals a novel trafficking determinant in the copper transporter ATP7B | PNAS
ATP7B Gene - GeneCards | ATP7B Protein | ATP7B Antibody
