Germ-line deletions of mtDNA in mitochondrial myopathy.

mtDNA encodes subunits of the electron transport chain and is exclusively maternally inherited in mammals. It has been suggested that mtDNA might be the site of some of the mutations causing a group of human disorders called the "mitochondrial myopathies," because these may both be (1) acc...

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Bibliografiske detaljer
Main Authors: Poulton, J, Deadman, M E, Ramacharan, S, Gardiner, R M
Format: Artigo
Sprog:Inglês
Udgivet: 1991
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682963/
https://ncbi.nlm.nih.gov/pubmed/2014792
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