Population
mdx mouse model of Duchenne muscular dystrophy
Design
Review
Authors
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Caution needed extrapolating mdx data to human DMD; leaves open validation via human-relevant models.
Awareness of inter-species differences, particularly in scale and biological mechanisms, is crucial to avoid misjudging the applicability of results from mdx mouse models to human Duchenne muscular dystrophy.
Terence A. Partridge (2013) studied this question.
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