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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Detalles Bibliográficos
Autores principales: Finsterer, Josef, Zarrouk-Mahjoub, Sinda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852432/
https://www.ncbi.nlm.nih.gov/pubmed/29385732
http://dx.doi.org/10.3390/jcm7020016

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852432/
https://www.ncbi.nlm.nih.gov/pubmed/29385732
http://dx.doi.org/10.3390/jcm7020016

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