A meta-analysis and systematic review of Leigh syndrome: clinical manifestations, respiratory chain enzyme complex deficiency, and gene mutations

Leigh syndrome (also called Leigh disease or subacute necrotizing encephalomyelopathy) is a rare inherited neurometabolic disorder, which affects the central nervous system. This meta-study systematically analyzed clinical manifestations, respiratory chain enzyme complex deficiency, and gene mutatio...

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Detalles Bibliográficos
Autores principales: Chang, Xueli, Wu, Yaxin, Zhou, Jie, Meng, Huaxing, Zhang, Wei, Guo, Junhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
5300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004636/
https://www.ncbi.nlm.nih.gov/pubmed/32000367
http://dx.doi.org/10.1097/MD.0000000000018634

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004636/
https://www.ncbi.nlm.nih.gov/pubmed/32000367
http://dx.doi.org/10.1097/MD.0000000000018634

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