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Neurological Wilson’s Disease Signs—Hepatic Encephalopathy or Copper Toxicosis?
Wilson’s disease (WD) is a rare autosomal recessive (AR) disorder resulting from mutations in the ATP7B gene, which is responsible for the encryption of transmembrane copper transporting ATPase. The symptomatic presentation of the disease is estimated to be about 1 in 30,000. The impairment of ATP7B...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10001333/ https://www.ncbi.nlm.nih.gov/pubmed/36900037 http://dx.doi.org/10.3390/diagnostics13050893 |