Population
Mice with disrupted skeletal actin gene by homologous recombination, hemizygous, and wild-type littermates
Comparison
Disruption of the skeletal actin gene vs Wild-type and hemizygous littermates
Design
Preclinical
Follow-up
neonatal period (day 1 to 9)
Authors
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Does not alter clinical practice; leaves open actin isoform compensation in human myopathy models.
Skeletal actin is essential for adequate skeletal muscle growth, function, and postnatal survival in mice, and its loss cannot be fully compensated by cardiac and vascular smooth-muscle actin.
Crawford et al. (2002) studied this question.