OMIA:000699-93934 : Myotonic dystrophy in Coturnix japonica (Japanese quail) |
Categories: Muscle phene
Possibly relevant human trait(s) and/or gene(s) (MIM number): 160900 (trait)
Links to MONDO diseases: No links.
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal dominant
Considered a defect: yes
Key variant known: no
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. (2013). OMIA:000699-93934: 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 | 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