You are here: OMIA / Search / OMIA 000699 / Japanese quail

OMIA 000699-93934 : Myotonic dystrophy in Coturnix japonica

Possibly relevant human trait(s) and/or gene(s) (MIM number): 160900

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal Dominant

Considered a defect: yes

Key variant known: no

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 Tanaka, S., Braga, I.S., Kimura, T., Ochiai, K., Itakura, C., Mizutani, M. :
Inherited muscular disorder in mutant Japanese quail (Coturnix coturnix japonica) - an ultrastructural study Journal of Comparative Pathology 114:325-337, 1996. Pubmed reference: 8762590.
Tanaka, S., Braga, I.S., Kimura, T., Ochiai, K., Itakura, C., Mizutani, M. :
Inherited muscular disorder in mutant Japanese quail (Coturnix coturnix japonica) - an immunohistochemical study Journal of Comparative Pathology 115:139-150, 1996. Pubmed reference: 8910742.
1995 Braga, I.S., Oda, K., Kikuchi, T., Tanaka, S., Shin, Y., Sento, M., Itakura, C., Mizutani, M. :
New inherited muscular disorder in Japanese quails (Coturnix coturnix japonica) Veterinary Pathology 32:351-360, 1995. Pubmed reference: 7483209.

Edit History


  • Created by Frank Nicholas on 06 Sep 2005
  • Changed by Frank Nicholas on 05 Aug 2013