Associated Papers
An Update on Reported Variants in the Skeletal Muscle α-Actin (ACTA1) Gene.
Clayton JS et al.
Human Mutation, 2024
40225930 (PubMed )
Supplement: 6496088.f1.docx
New aspects of myofibrillar myopathies.
Kley RA et al.
Current Opinion in Neurology, 2016
Severe congenital actin related myopathy with myofibrillar myopathy features.
Selcen D
Neuromuscular Disorders : Nmd, 2015
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