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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Int J Med Sci
Päätekijät: Germain, Nicolas, Dessein, Anne-Frédérique, Vienne, Jean-Claude, Dobbelaere, Dries, Mention, Karine, Joncquel, Marie, Dekiouk, Salim, Laine, William, Kluza, Jérome, Marchetti, Philippe
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Ivyspring International Publisher 2019
Aiheet:
Research Paper
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6643127/
https://ncbi.nlm.nih.gov/pubmed/31341406
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7150/ijms.32413
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