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Mutations in repeating structural motifs of tropomyosin cause gain of function in skeletal muscle myopathy patients

✍ Scribed by Marston, S.; Memo, M.; Messer, A.; Papadaki, M.; Nowak, K.; McNamara, E.; Ong, R.; El-Mezgueldi, M.; Li, X.; Lehman, W.

No coin nor oath required. For personal study only.

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