Index | PMID | Date | Reference |
---|---|---|---|
1 | 10621222 | 2000 | Shin, W. S., Tanaka, M., Suzuki, J., Hemmi, C., Toyo-Oka, T. (2000) A novel homoplasmic mutation in mtDNA with a single evolutionary origin as a risk factor for cardiomyopathy American Journal of Human Genetics . 67 (6): 1617-1620 . |
2 | 12560876 | 2003 | Mimaki, M., Ikota, A., Sato, A., Komaki, H., Akanuma, J., Nonaka, I., Goto, Y. (2003) A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy Journal of Human Genetics . 48 (1): 47-50 . |