Clinical, neuroimaging, biochemical, and genetic features in six Chinese patients with Adrenomyeloneuropathy

BACKGROUND: Adrenoleukodystrophy is a rare neurogenetic disease, AMN is the most common adult phenotype, such patients in China have not gotten enough attention. This article aims to study the features of AMN in Chinese patients and expand the gene spectrum of Chinese X-linked adrenoleukodystrophy (...

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Detalles Bibliográficos
Autores principales: Li, Jie, Wang, Hongfen, He, Zizi, Wang, Xiangqing, Tang, Jing, Huang, Dehui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745787/
https://www.ncbi.nlm.nih.gov/pubmed/31526374
http://dx.doi.org/10.1186/s12883-019-1449-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745787/
https://www.ncbi.nlm.nih.gov/pubmed/31526374
http://dx.doi.org/10.1186/s12883-019-1449-5

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