Loss of Myelin-Associated Glycoprotein in Kearns-Sayre Syndrome

OBJECTIVE: To explore myelin components and mitochondrial changes within the central nervous system in patients with well-characterized mitochondrial disorders due to nuclear DNA or mitochondrial DNA (mtDNA) mutations. DESIGN: Immunohistochemical analysis, histochemical analysis, mtDNA sequencing, a...

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Bibliografiska uppgifter
Huvudupphovsmän: Lax, Nichola Z., Campbell, Graham R., Reeve, Amy K., Ohno, Nobuhiko, Zambonin, Jessica, Blakely, Emma L., Taylor, Robert W., Bonilla, Eduardo, Tanji, Kurenai, DiMauro, Salvatore, Jaros, Evelyn, Lassmann, Hans, Turnbull, Doug M., Mahad, Don J.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2012
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3672633/
https://ncbi.nlm.nih.gov/pubmed/22491194
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archneurol.2011.2167
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