| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 11119722 | 2000 | Carrozzo, R., Murray, J., Santorelli, F. M., Capaldi, R. A. (2000) The T9176G mutation of human mtDNA gives a fully assembled but inactive ATP synthase when modeled in Escherichia coli FEBS Letters . 486 (3): 297-299 . |
| 2 | 11382202 | 2000 | Carrozzo, R., Murray, J., Capuano, O., Tessa, A., Chichierchia, G., Neglia, M. R., Capaldi, R. A., Santorelli, F. M. (2000) A novel mtDNA mutation in the ATPase6 gene studied by E. coli modeling Neurological Sciences . 21 (5 Suppl): S983-984 . |
| 3 | 11731285 | 2002 | Akagi, M., Inui, K., Tsukamoto, H., Sakai, N., Muramatsu, T., Yamada, M., Matsuzaki, K., Goto, Y., Nonaka, I., Okada, S. (2002) A point mutation of mitochondrial ATPase 6 gene in Leigh syndrome Neuromuscular Disorders 12 (1): 53-55 . |
| 4 | 18402672 | 2008 | Alvarez-Iglesias, V., Barros, F., Carracedo, A., Salas, A. (2008) Minisequencing mitochondrial DNA pathogenic mutations [METHODS] BMC Medical Genetics . 9 (-): 26 . |