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Biomarkers for Detecting Mitochondrial Disorders

(1) Objectives: Mitochondrial disorders (MIDs) are a genetically and phenotypically heterogeneous group of slowly or rapidly progressive disorders with onset from birth to senescence. Because of their variegated clinical presentation, MIDs are difficult to diagnose and are frequently missed in their...

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Detaylı Bibliyografya
Yayımlandı:J Clin Med
Asıl Yazarlar: Finsterer, Josef, Zarrouk-Mahjoub, Sinda
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: MDPI 2018
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5852432/
https://ncbi.nlm.nih.gov/pubmed/29385732
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm7020016
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