OMIA 000344-9986 : Epilepsy in Oryctolagus cuniculus

In other species: cattle , chicken , dog , domestic cat , Mongolian gerbil , horse , golden hamster

Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 104130 , 117100 , 121200 , 121201 , 125370 , 132090 , 132100 , 132300 , 159600 , 182610 , 203600 , 208700 , 220300 , 226750 , 226800 , 226810 , 226850 , 254770 , 254780 , 254800 , 266270 , 267740 , 270805 , 301900 , 310370 , 545000 , 600131 , 600143 , 600512 , 600513 , 600669 , 601068 , 245570

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal Recessive

Considered a defect: yes

Key variant known: no

Species-specific symbol: ep

Species-specific description: See Robinson (1958, pp. 331-333).

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.
1979 Consroe, P., Edmonds, H.L. :
Genetic animal models of epilepsy. Introduction. Fed Proc 38:2397-8, 1979. Pubmed reference: 478016.
1958 Robinson, R. :
Genetic studies of the rabbit. Bibliographia Genetica 17:229–558, 1958.
1957 Pobisch, R. :
Familial epileptiform disease in a breed of rabbits Wiener Tierärztliche Monatsschrift 44:193-199, 1957.
1955 Sawin, P.B. :
Recent genetics of the domestic rabbit. Adv Genet 7:183-226, 1955. Pubmed reference: 13258375.

Edit History


  • Created by Frank Nicholas on 06 Sep 2005
  • Changed by Frank Nicholas on 27 Nov 2011
  • Changed by Frank Nicholas on 29 Apr 2016