Characteristics of neurological Wilson’s disease with corpus callosum abnormalities

BACKGROUND: Wilson’s disease (WD) is an autosomal recessive disease of impaired copper metabolism. Previous study demonstrated that WD with corpus callosum abnormalities (WD-CCA) was limited to the posterior part (splenium). This study aimed to compare clinical features between WD-CCA and WD without...

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Detalles Bibliográficos
Autores principales: Zhou, Zhi-Hua, Wu, Yun-Fan, Cao, Jin, Hu, Ji-Yuan, Han, Yong-Zhu, Hong, Ming-Fan, Wang, Gong-Qiang, Liu, Shu-Hu, Wang, Xue-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499990/
https://www.ncbi.nlm.nih.gov/pubmed/31053106
http://dx.doi.org/10.1186/s12883-019-1313-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499990/
https://www.ncbi.nlm.nih.gov/pubmed/31053106
http://dx.doi.org/10.1186/s12883-019-1313-7

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