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对线粒体医学会原发性线粒体病患者管理标准专家共识的解读
Primary mitochondrial disease is the most common inborn error of metabolism and is highly heterogeneous in terms of clinical manifestations and inheritance pattern. It has high mortality and disability rates. Multiple systems are often involved in this disease, and it is necessary to perform compreh...
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| Publicado en: | Zhongguo Dang Dai Er Ke Za Zhi |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
中国当代儿科杂志编辑部
2018
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7389018/ https://ncbi.nlm.nih.gov/pubmed/30477617 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7499/j.issn.1008-8830.2018.11.002 |
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