Associated Papers
Structural and functional mechanisms of actin isoforms.
Heissler SM et al.
The Febs Journal, 2025
38779987 (PubMed )
Supplement: FEBS-292-468-s001.pdf
Insights into the effects of disease-causing mutations in human actins.
Rubenstein PA et al.
Cytoskeleton (hoboken, N.j.), 2014
Functional analysis of a de novo ACTB mutation in a patient with atypical Baraitser-Winter syndrome.
Johnston JJ et al.
Human Mutation, 2013
Genotype-phenotype correlations in ACTA1 mutations that cause congenital myopathies.
Feng JJ et al.
Neuromuscular Disorders : Nmd, 2009
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