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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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Detaylı Bibliyografya
Yayımlandı:Zhongguo Dang Dai Er Ke Za Zhi
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 中国当代儿科杂志编辑部 2018
Konular:
Online Erişim: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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