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Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouse

Published online by Cambridge University Press:  14 April 2009

M. S. Deol  and
Margaret C. Green
M. S. Deol
Affiliation:
The Jackson Laboratory, Bar Harbor, Maine
Margaret C. Green
Affiliation:
The Jackson Laboratory, Bar Harbor, Maine
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A new recessive gene affecting behaviour and the inner ear in the mouse has been discovered. It was named Snell's waltzer, and assigned the symbol sv. It is in linkage group II, about two map units from short ear (se) on the side opposite to that of luxoid (lu). The behaviour of sv/sv mice closely resembles that of other members of the shaker-waltzer group. The abnormalities of the inner ear consist in degeneration of certain parts following normal morphogenesis. The entire neuro-epithelium —that is, the organ of Corti, the two maculae and the three cristae—is affected, and this feature distinguishes it from other degenerative type mutants of this group.

Type
Research Article
Information
Genetics Research , Volume 8 , Issue 3 , December 1966 , pp. 339 - 345
Copyright
Copyright © Cambridge University Press 1966

References

REFERENCES

Deol, M. S. (1954). The anomalies of the labyrinth of the mutants varitint-waddler, shaker-2 and jerker in the mouse. J. Genet. 52, 562–588.CrossRefGoogle Scholar
Deol, M. S. (1956). The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse. Proc. R. Soc. B, 145, 206–213.Google ScholarPubMed
Deol, M. S. (1966). The probable mode of gene action in the circling mutants of the mouse. Genet. Res. Camb. 7, 363–371.CrossRefGoogle ScholarPubMed
Green, M. C. (1961). The position of luxoid in linkage group II of the mouse. J. Hered. 52, 297–300.CrossRefGoogle ScholarPubMed
Grüneberg, H. (1956). Hereditary lesions of the labyrinth in the mouse. Brit. med. Bull. 12, 153–157.CrossRefGoogle ScholarPubMed
Sidman, R. L., Green, M. C. & Appel, S. H. (1965). Catalog of the Neurological Mutants of the Mouse. Cambridge: Harvard University Press.CrossRefGoogle Scholar