Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanisms.

Forty per cent of patients with mitochondrial myopathies, a diverse group of multisystem diseases predominantly affecting skeletal muscle and the brain, have large deletions of a proportion of muscle mitochondrial DNA (mt DNA). These appeared to be identical in 13 of 28 cases, contained within the r...

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Veröffentlicht in:	Nucleic Acids Res
Hauptverfasser:	Holt, I J, Harding, A E, Morgan-Hughes, J A
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	Oxford University Press 1989
Online-Zugang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC318006/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2748329/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/17.12.4465
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