| Literature DB >> 939913 |
P W Lane, T C Beamer, D D Myers.
Abstract
A new recessive mutation, myd, causing a diffuse and progressive myopathy in the mouse is described. Histopathological comparisons with normal littermates showed widely distributed focal lesions in all skeletal muscles of myd/myd. Body and organ weights of affected mice were considerably less than those of normal littermates and the mean lifespan of myodystrophic mice that survived weaning was 17 weeks with a range of 5 to 39 weeks. Myodystrophy is located on chromosome 8; it is linked to Os with about 6 percent and to Eso with about 37 percent recombination.Entities:
Mesh:
Year: 1976 PMID: 939913 DOI: 10.1093/oxfordjournals.jhered.a108687
Source DB: PubMed Journal: J Hered ISSN: 0022-1503 Impact factor: 2.645