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P2.23 Congenital form of X-linked myopathy with excessive autophagy associated with VMA21 mutation

✍ Scribed by C. Ikeda; R. Honda; H. Komaki; M. Sasaki; I. Munteanu; N. Ramachandran; B.A. Minassian; R. Tsuburaya; Y.K. Hayashi; I. Nishino

No coin nor oath required. For personal study only.

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