OMIA:001228-10042 : Spherocytosis in Peromyscus maniculatus (North American deer mouse)
Categories: Haematopoietic system phene
Links to MONDO diseases: No links.
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal recessive
Considered a defect: yes
Key variant known: no
Cite this entry
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 .|
- Created by Frank Nicholas on 06 Sep 2005