Clinical and genetic characterization of pediatric patients with Wilson’s disease from Yunnan province where ethnic minorities gather

Background: Wilson’s disease (WD) is an autosomal recessive disease that is caused by mutations in the ATP7B (a copper-transporting P-type ATPase) gene. The disease has a low prevalence and is characterized by a copper metabolism disorder. However, various characteristics of the disease are determin...

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Bibliografiske detaljer

Principais autores:	Yanjun Wang, Jiahui Fang, Bin Li, Chongyang Li, Shan Liu, Juan He, Lvyan Tao, Cuifen Li, Ya Yang, Li Li, Shufang Xiao
Format:	Artigo
Sprog:	Inglês
Udgivet:	Frontiers Media S.A. 2023-03-01
Serier:	Frontiers in Genetics
Fag:	Wilson’s disease pediatric patients ATP7B genetic characterization ethnic minorities
Online adgang:	https://www.frontiersin.org/articles/10.3389/fgene.2023.1142968/full
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