Conditional Knockout of the Menkes Disease Copper Transporter Demonstrates Its Critical Role in Embryogenesis | PLOS ONE
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ATP7A-related copper transport diseases—emerging concepts and future trends | Nature Reviews Neurology
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ATP7A and ATP7B copper transporters have distinct functions in the regulation of neuronal dopamine-β-hydroxylase - ScienceDirect
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ATP7A Clinical Genetics Resource – A comprehensive clinically annotated database and resource for genetic variants in ATP7A gene - ScienceDirect
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The contribution of copper efflux transporters ATP7A and ATP7B to chemoresistance and personalized medicine in ovarian cancer - ScienceDirect
![ATP7A pathogenic variants reported in this study. ATP7A consists of six... | Download Scientific Diagram ATP7A pathogenic variants reported in this study. ATP7A consists of six... | Download Scientific Diagram](https://www.researchgate.net/publication/334437291/figure/fig3/AS:780014798794753@1562981428609/ATP7A-pathogenic-variants-reported-in-this-study-ATP7A-consists-of-six-amino-terminal.png)
ATP7A pathogenic variants reported in this study. ATP7A consists of six... | Download Scientific Diagram
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An Overview and Update of ATP7A Mutations Leading to Menkes Disease and Occipital Horn Syndrome - Tümer - 2013 - Human Mutation - Wiley Online Library
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Metallothioneins regulate ATP7A trafficking and control cell viability during copper deficiency and excess | Scientific Reports
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The copper-transporting capacity of ATP7A mutants associated with Menkes disease is ameliorated by COMMD1 as a result of improved protein expression | Cellular and Molecular Life Sciences
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