Toxic accumulation of copper and neuropsychiatric symptoms due to a familial tunisian compound heterozygous ATP7B missense mutation

INTRODUCTION: Wilson disease (WD) is an autosomal recessive genetic disorder caused by loss-of-function mutations in the P-type copper ATPase, ATP7B (ATPase copper-transporting beta), which transports copper out of cells. It is characterized by toxic accumulation of copper primarily in the liver and...

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Detalles Bibliográficos
Autor principal: Abdelmoula, N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2021
Materias:
Abstract
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9480414/
http://dx.doi.org/10.1192/j.eurpsy.2021.1901

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9480414/
http://dx.doi.org/10.1192/j.eurpsy.2021.1901

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