References in periodicals archive ?
A de novo dominant mutation in ACTA1 causing congenital nemaline myopathy associated with a milder phenotype: expanding the spectrum of dominant ACTA1 mutations.
Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation.
However during development, the skeletal form, ACTA1, increases in production and by birth has taken over.
monocytogenes based on genetic loci in several genes: the hemolysin (hlyA), internalin (inlA), positive regulatory factor (prfA), and actin polymerization (actA1, actA2) genes.