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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Detalles Bibliográficos
Autores principales: Mancuso, Michelangelo, Montano, Vincenzo, Orsucci, Daniele, Peverelli, Lorenzo, Caputi, Luigi, Gambaro, Paola, Siciliano, Gabriele, Lamperti, Costanza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021764/
https://www.ncbi.nlm.nih.gov/pubmed/27656415
http://dx.doi.org/10.1016/j.ymgmr.2016.08.010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021764/
https://www.ncbi.nlm.nih.gov/pubmed/27656415
http://dx.doi.org/10.1016/j.ymgmr.2016.08.010

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