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Transcranial sonography changes in heterozygotic carriers of the ATP7B gene

PURPOSE: Wilson’s disease (WD) is an autosomal recessive disorder of ATP7B gene leading to impaired copper metabolism. Brain imaging, such as magnetic resonance (MR) and transcranial sonography (TCS) in WD patients, shows changes mostly in the basal ganglia. Heterozygotic carriers of one faulty ATP7...

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Detalhes bibliográficos
Publicado no:Neurol Sci
Main Authors: Skowronska, Marta, Litwin, Tomasz, Kurkowska-Jastrzębska, Iwona, Członkowska, Anna
Formato: Artigo
Idioma:Inglês
Publicado em: Springer International Publishing 2020
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7419484/
https://ncbi.nlm.nih.gov/pubmed/32270360
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10072-020-04378-6
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