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ACTA1Actin, Alpha, Skeletal Muscle 1
References in periodicals archive ?
However during development, the skeletal form, ACTA1, increases in production and by birth has taken over.
The researchers suggested that mutations to the ACTA1 gene cause a rare but serious myopathy or muscular disease.
Lead researcher Nowak showed that mice lacking ACTA1 died within nine days after birth.