| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 1315844 | 1992 | Hammans, S.R., Sweeney, M.G., Holt, I.J., Cooper, J.M., Toscano, A., Clark, J.B., Morgan-Hughes, J.A., Harding, A.E. (1992) Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathy Journal of the Neurological Sciences . 107 (1): 87-92 . |
| 2 | 1606473 | 1992 | Hammans, S.R., Sweeney, M.G., Wicks, D.A., Morgan-Hughes, J.A., Harding, A.E. (1992) A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathies Brain . 115 (Pt 2): 343-365 . |
| 3 | 8423892 | 1993 | Herzberg, N.H., van Schooneveld, M.J., Bleeker-Wagemakers, E.M., Zwart, R., Cremers, F.P., van der Knaap, M.S., Bolhuis, P.A., deVisser, M. (1993) Kearns-Sayre syndrome with a phenocopy of choroideremia instead of pigmentary retinopathy Neurology . 43 (1): 218-221 . |
| 4 | 18414780 | 2008 | Yamashita, S., Nishino, I., Nonaka, I., Goto, Y. (2008) Genotype and phenotype analyses in 136 patients with single large-scale mitochondrial DNA deletions Journal of Human Genetics . 53 (7): 598-606 . |