Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoforms.

We have studied a cohort of nemaline myopathy (NM) patients with mutations in the muscle alpha-skeletal actin gene (ACTA1). Immunoblot analysis of patient muscle demonstrates increased gamma-filamin, myotilin, desmin and alpha-actinin in many NM patients, consistent with accumulation of Z line-deriv...

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Bibliographic Details
Main Authors: Ilkovski, B, Nowak, K, Domazetovska, A, Maxwell, A, Clement, S, Davies, K, Laing, N, North, K, Cooper, S
Format: Journal article
Language:English
Published: 2004