OMIA:000011-9986 : Paresis, posterior in Oryctolagus cuniculus (rabbit) |
In other species: dog
Categories: Nervous system phene
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal recessive
Disease-related: yes
Key variant known: no
Species-specific description: See Robinson (1958, p. 335).
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2016). OMIA:000011-9986: 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.
1958 | Robinson, R. : |
Genetic studies of the rabbit. Bibliographia Genetica 17:229–558, 1958. | |
1937 | Nachtsheim, H. : |
Erbpathologische Untersuchungen am Kaninchen [Investigation of inherited defects in rabbits] Z. indo Abst. u. Vererbgs 73:463-466, 1937. DOI: 10.1007/BF01847500. |
Edit History
- Created by Frank Nicholas on 03 May 2016
- Changed by Frank Nicholas on 03 May 2016