Mutations of the slow muscle α-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy

D. Wattanasirichaigoon, K. J. Swoboda, F. Takada, H. Q. Tong, V. Lip, S. T. Iannaccone, C. Wallgren-Pettersson, N. G. Laing, Allan H. Beggs

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