OMIA:000966-9986 : Systematic mitochondrial heteroplasmy in Oryctolagus cuniculus (rabbit)

Categories: Cellular phene

Links to MONDO diseases: No links.

Mendelian trait/disorder: unknown

Considered a defect: unknown

Genetic engineering: Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing

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