Lataa...
Pathomechanisms in Coenzyme Q(10)-Deficient Human Fibroblasts
Primary coenzyme Q(10) (CoQ(10)) deficiency is a rare mitochondrial disorder associated with 5 major clinical phenotypes: (1) encephalomyopathy, (2) severe infantile multisystemic disease, (3) cerebellar ataxia, (4) isolated myopathy, and (5) steroid-resistant nephrotic syndrome. Growth retardation,...
Tallennettuna:
| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
S. Karger AG
2014
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4112524/ https://ncbi.nlm.nih.gov/pubmed/25126049 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000360494 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|