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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
Research output: Contribution to journal › Article › peer-review
76
Scopus
citations