Key points are not available for this paper at this time.
Respiratory chain dysfunction is an important contributor to human pathology (1–3). The generation of animal models has much facilitated in-depth studies of pathogenetic mechanisms in mitochondrial disease (4). The function of the respiratory chain is subject to the dual genetic control of both the nuclear and mitochondrial genomes (1).
Ekstrand et al. (Fri,) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: