Abstract
SINCE the ætiopathology of muscular dystrophy is still unsettled, wide interest was provoked by the recent elaboration of a mouse strain afflicted with a hereditary myopathy resembling in many respects the human disease. This condition, referred to as dystrophia muscularis, arose as a mutation in a colony of inbred strain 129 mice and the inheritance of the disease has been shown to follow the pattern of an autosomal recessive gene1. Although the symptomatology and pathology of dystrophia muscularis has been described in detail1–4, occurrence of cardiac lesions has never been mentioned. Moreover, it was emphasized that the phenotypic effects of this mutation are restricted to skeletal muscular tissue5, in which the well-known and characteristic abnormalities progressively develop.
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JASMIN, G., BAJUSZ, E. Myocardial Lesions in Strain 129 Dystrophic Mice. Nature 193, 181–182 (1962). https://doi.org/10.1038/193181a0
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DOI: https://doi.org/10.1038/193181a0
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