SLC25A4 and C10ORF2 Mutations in Autosomal Dominant Progressive External Ophthalmoplegia

BACKGROUND AND PURPOSE: Progressive external ophthalmoplegia (PEO) with Mendelian inheritance is a heterogeneous group of diseases associated with multiple deletions of mitochondrial DNA (mtDNA), which results from the disturbed replication and maintenance of mtDNA secondary to the mutations of nucl...

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Detalles Bibliográficos
Autores principales: Park, Kyung-Pil, Kim, Hyang-Sook, Kim, Eun-Sook, Park, Young-Eun, Lee, Chang-Hoon, Kim, Dae-Seong
Formato: Texto
Lenguaje:English
Publicado: Korean Neurological Association 2011
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3079156/
https://www.ncbi.nlm.nih.gov/pubmed/21519523
http://dx.doi.org/10.3988/jcn.2011.7.1.25

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3079156/
https://www.ncbi.nlm.nih.gov/pubmed/21519523
http://dx.doi.org/10.3988/jcn.2011.7.1.25

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