Metabolomic profiling of Wilson disease, an inherited disorder of copper metabolism, and diseases with similar symptoms but normal copper metabolism

BACKGROUND: Wilson’s disease (WD) is a hereditary disorder that results in the accumulation of copper. The pathogenic mechanism is not well understood, and diagnosing the disease can be challenging, as it shares similarities with more prevalent conditions. To explore the metabolomic features of WD a...

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Detalles Bibliográficos
Autores principales: Qiu, Yijie, Su, Mingchuan, Xiao, Xina, Zhou, Dingzi, Xie, Linshen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10494341/
https://www.ncbi.nlm.nih.gov/pubmed/37697371
http://dx.doi.org/10.1186/s13023-023-02900-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10494341/
https://www.ncbi.nlm.nih.gov/pubmed/37697371
http://dx.doi.org/10.1186/s13023-023-02900-5

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