First-line Screening of OXPHOS Deficiencies Using Microscale Oxygraphy in Human Skin Fibroblasts: A Preliminary Study

The diagnosis of mitochondrial diseases is a real challenge because of the vast clinical and genetic heterogeneity. Classically, the clinical examination and genetic analysis must be completed by several biochemical assays to confirm the diagnosis of mitochondrial disease. Here, we tested the validi...

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Detalles Bibliográficos
Autores principales: Germain, Nicolas, Dessein, Anne-Frédérique, Vienne, Jean-Claude, Dobbelaere, Dries, Mention, Karine, Joncquel, Marie, Dekiouk, Salim, Laine, William, Kluza, Jérome, Marchetti, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2019
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643127/
https://www.ncbi.nlm.nih.gov/pubmed/31341406
http://dx.doi.org/10.7150/ijms.32413

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643127/
https://www.ncbi.nlm.nih.gov/pubmed/31341406
http://dx.doi.org/10.7150/ijms.32413

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