OMIA:000966-9986 : Systematic mitochondrial heteroplasmy in Oryctolagus cuniculus |
Categories: Cellular phene
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: unknown
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2022). OMIA:000966-9986: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
References
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
| 1996 | Dufresne, C., Mignotte, F., Guéride, M. : |
| The presence of tandem repeats and the initiation of replication in rabbit mitochondrial DNA. Eur J Biochem 235:593-600, 1996. Pubmed reference: 8654406 . DOI: 10.1111/j.1432-1033.1996.00593.x. | |
| 1994 | Casane, D., Dennebouy, N., Derochambeau, H., Mounolou, J.C., Monnerot, M. : |
| Genetic analysis of systematic mitochondrial heteroplasmy in rabbits Genetics 138:471-480, 1994. Pubmed reference: 7828828 . |
Edit History
- Created by Frank Nicholas on 06 Sep 2005
- Changed by Imke Tammen2 on 21 Oct 2022