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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...
Autores principales: | Chang, Xueli, Wu, Yaxin, Zhou, Jie, Meng, Huaxing, Zhang, Wei, Guo, Junhong |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
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Materias: | |
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 |
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