Key result
This corrigendum corrects the predicted protein change for the LMOD3 mutation c.601_602delGA to p.D201Qfs*9 and the notation for p.S47Qfs*13 in a case series of patients with nemaline myopathy.
This corrigendum corrects specific LMOD3 mutation descriptions in a study of nemaline myopathy.
Corrects LMOD3 variant annotations in nemaline myopathy cases; leaves open accuracy of prior genetic reports and database entries.
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Yuen et al. (2015) studied Nemaline myopathy (n=21). LMOD3 mutations was evaluated. This corrigendum corrects the predicted protein change for the LMOD3 mutation c.601_602delGA to p.D201Qfs*9 and the notation for p.S47Qfs*13 in a case series of patients with nemaline myopathy.
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