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Glucose metabolism derangements in adults with the MELAS m.3243A>G mutation
The m.3243A>G mutation in the mitochondrial gene MT-TL1 leads to a wide clinical spectrum ranging from asymptomatic carriers to MELAS (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes) at the severe end. Diabetes mellitus (DM) occurs in mitochondrial diseases, with the m...
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| Publicat a: | Mitochondrion |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4252755/ https://ncbi.nlm.nih.gov/pubmed/25086207 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mito.2014.07.008 |
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