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Clinical Presentations of Coenzyme Q(10) Deficiency Syndrome
Coenzyme Q(10) (CoQ(10)) deficiency is a clinically and genetically heterogeneous syndrome which has been associated with 5 major clinical phenotypes: (1) encephalomyopathy, (2) severe infantile multisystemic disease, (3) nephropathy, (4) cerebellar ataxia, and (5) isolated myopathy. Of these phenot...
Tallennettuna:
| Päätekijät: | , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
S. Karger AG
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4112523/ https://ncbi.nlm.nih.gov/pubmed/25126046 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000360490 |
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