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ArticleIranian journal of neurology2015

Mutation analysis in exons 22 and 24 of SCN4A gene in Iranian patients with non-dystrophic myotonia.

Mohammad Mehdi Heidari et al.PubMed ↗Full text ↗

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Mutation analysis in exons 22 and 24 of SCN4A gene in Iranian patients with non-dystrophic myotonia. | OpenQuestion