| 1 |
15120634
| 2004 |
Ruppert, V., Nolte, D., Aschenbrenner, T., Pankuweit, S., Funck, R., Maisch, B. (2004) Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome Biochemical and Biophysical Research Communications . 318 (2): 535-543 . |
| 2 |
19220304
| 2009 |
Zaki, E. A., Freilinger, T., Klopstock, T., Baldwin, E. E., Heisner, K. R., Adams, K., Dichgans, M., Wagler, S., Boles, R. G. (2009) Two common mitochondrial DNA polymorphisms are highly associated with migraine headache and cyclic vomiting syndrome Cephalalgia . 29 (7): 719-728 . |
| 3 |
22879922
| 2012 |
Achilli, A., Iommarini, L., Olivieri, A., Pala, M., Kashani, B. H., Reynier, P., La Morgia, C., Valentino, M. L., Liguori, R., Pizza, F., Barboni, P., Sadun, F., De Negri, A., Zeviani, M., Dollfus, H., Moulignier, A., Ducos, G., Orssaud, C., Bonneau, D., Procaccio, V., Leo-Kottler, B., Fauser, S., Wissinger, B., Amati-Bonneau, P., Torroni, A., Carelli, V. (2012) Rare primary mitochondrial DNA mutations and synergistic variants in Leber's hereditary optic neuropathy PLOS One . 7 (8): e42242 . |