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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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| Publicado no: | Mitochondrion |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | 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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