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Wilson's disease: A rare autosomal recessive disorder of copper metabolism, causing copper accumulation in various organs, especially the liver and brain. ✓Genetics: 🔹Mutation in the ATP7B gene on chromosome 13. 🔹Impaired hepatic

However, present approaches of theoretical calculation are usually built upon TBC-based theories, showing huge limitations in accurately describing the electronic structure of aggregates and related noncovalent couplings

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[DOI] [Google Scholar] 101.McMahon S., Kennedy R., Duffy P., Vasquez J.M., Wall J.G., Tai H., Wang W