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Mitochondrial m.3243A > G mutation and carotid artery dissection
The common m.3243A > G mutation of the mitochondrial DNA tRNALeu (UUR) gene is a maternally inherited mutation causing a wide spectrum of neurological and multisystemic disorders, including MELAS, characterized by recurrent cerebral infarction from young age. Vascular pathology in mitochondrial d...
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| Publicado no: | Mol Genet Metab Rep |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5021764/ https://ncbi.nlm.nih.gov/pubmed/27656415 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgmr.2016.08.010 |
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