Stimulation of Liver Fibrosis by N2 Neutrophils in Wilson’s Disease

BACKGROUND & AIMS: Wilson’s disease is an inherited hepatoneurologic disorder caused by mutations in the copper transporter ATP7B. Liver disease from Wilson’s disease is one leading cause of cirrhosis in adolescents. Current copper chelators and zinc salt treatments improve hepatic presentations...

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Detalles Bibliográficos
Autores principales: Mi, Xiaoxiao, Song, Yu, Deng, Chaohua, Yan, Jian, Li, Zhihui, Li, Yingniang, Zheng, Jun, Yang, Wenjun, Gong, Ling, Shi, Junping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514429/
https://www.ncbi.nlm.nih.gov/pubmed/37406734
http://dx.doi.org/10.1016/j.jcmgh.2023.06.012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514429/
https://www.ncbi.nlm.nih.gov/pubmed/37406734
http://dx.doi.org/10.1016/j.jcmgh.2023.06.012

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