OMIA 000011-9986 : Paresis, posterior in Oryctolagus cuniculus
In other species: dog Mendelian trait/disorder: yes Mode of inheritance: Autosomal Recessive Considered a defect: yes Key variant known: no Species-specific description: See Robinson (1958, p. 335).
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.|
- Created by Frank Nicholas on 03 May 2016
- Changed by Frank Nicholas on 03 May 2016