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P187 – 2088 A case of debilitating fluctuating myotonia due to autosomal dominant mutation in SCN4A gene

✍ Scribed by Gnidovec Strazisar, B; Writzl, K; Leonardis, L

No coin nor oath required. For personal study only.

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A new case of autosomal dominant myotoni

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G.P.3.04 Autosomal dominant Progressive

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