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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Detalles Bibliográficos
Autores principales: Skowronska, Marta, Litwin, Tomasz, Kurkowska-Jastrzębska, Iwona, Członkowska, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419484/
https://www.ncbi.nlm.nih.gov/pubmed/32270360
http://dx.doi.org/10.1007/s10072-020-04378-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419484/
https://www.ncbi.nlm.nih.gov/pubmed/32270360
http://dx.doi.org/10.1007/s10072-020-04378-6

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