doi: 10.1093/oxfordjournals.jhered.a108705.
Three recessive genes for congenital osteopetrosis in Norway rat
- PMID: 780413
- DOI: 10.1093/oxfordjournals.jhered.a108705
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Three recessive genes for congenital osteopetrosis in Norway rat
J Hered.
1976 May-Jun.
Abstract
In the rat, the autosomal recessive toothless (t1) mutation exhibits an acute form of osteopetrosis. This gene is not an allele of either ia or op that causes respectively, a transitory and acute form of the disease. Comparative radiographic study of t1/t1 and op/op mutants reveals some differences in respect to the size and shape of long bones. In contrast to op/op mutants, homozygous t1/t1 animals failed to respond to either parabiosis or bone marrow transplants.
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