Autor: |
Walker, John M., Copeland, William C., Ekstrand, Mats, Larsson, Nils-Göran |
Zdroj: |
Mitochondrial DNA; 2002, p391-400, 10p |
Abstrakt: |
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). [ABSTRACT FROM AUTHOR] |
Databáze: |
Supplemental Index |
Externí odkaz: |
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