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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Mol Genet Metab Rep
Päätekijät: Mancuso, Michelangelo, Montano, Vincenzo, Orsucci, Daniele, Peverelli, Lorenzo, Caputi, Luigi, Gambaro, Paola, Siciliano, Gabriele, Lamperti, Costanza
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier 2016
Aiheet:
Case Report
Linkit: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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