Actualización en el diagnóstico bioquímico de la enfermedad de Wilson

Actualización en el diagnóstico bioquímico de la enfermedad de Wilson

La enfermedad de Wilson (EW) es un trastorno hereditario del metabolismo del cobre causado por mutaciones en el gen ATP7B, en el que se produce la acumulación de este elemento en el hígado y otros órganos y tejidos de los pacientes afectados, provocando principalmente manifestaciones hepáticas y neu...

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Bibliographic Details
Main Authors:	Martínez-Morillo Eduardo, Bauça Josep Miquel
Format:	Article
Language:	English
Published:	De Gruyter 2022-05-01
Series:	Advances in Laboratory Medicine
Subjects:	ceruloplasmina cobre enfermedad de wilson gen atp7b
Online Access:	https://doi.org/10.1515/almed-2021-0089

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