OMIA:001228-10042 : Spherocytosis in Peromyscus maniculatus (North American deer mouse) |
In other species: dog , taurine cattle
Categories: Haematopoietic system phene
Links to possible relevant human trait(s) and/or gene(s) in OMIM: 109270 (gene) , 182900 (trait) , 612653 (trait)
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal recessive
Disease-related: yes
Key variant known: no
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:001228-10042: 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.
| 1967 | Steinmuller, D., Motulsky, A.G. : |
| Treatment of hereditary spherocytosis in Peromyscus by radiation and allogeneic bone marrow transplantation. Blood 29:320-30, 1967. Pubmed reference: 5335711. | |
| 1963 | Fitzpatrick, W.K., Burdette, W.J., Huestis, R.R. : |
| Cholelithiasis and spherocytosis in Peromyscus. Arch Surg 86:897-903, 1963. Pubmed reference: 13945379. | |
| 1960 | Anderson, R., Huestis, R.R., Motulsky, A.G. : |
| Hereditary spherocytosis in the deer mouse. Its similarity to the human disease. Blood 15:491-504, 1960. Pubmed reference: 13793441. |
Edit History
- Created by Frank Nicholas on 06 Sep 2005