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Liver Failure of Wilson's Disease With Manifestations Similar to Porphyria and Uncommon ATP7B Gene Mutation: A Case Report and Literature Review

Background: Wilson's disease (WD) is a rare condition; its diagnosis is challenging owing to a wide spectrum of ATP7B genotypes and variable clinical phenotypes, along with environmental factors. Few cases of WD with presentation of skin lesions and acute neurovisceral symptoms have been report...

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Detalles Bibliográficos
Autores principales:	Zou, Ju, Wang, Ying-Hao, Wang, Ling, Chen, Ruo-Chan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350053/ https://www.ncbi.nlm.nih.gov/pubmed/34381801 http://dx.doi.org/10.3389/fmed.2021.702312

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