Mutations of the slow muscle α-tropomyosin gene, <i>TPM3</i> , are a rare cause of nemaline myopathy
Duangrurdee Wattanasirichaigoon(Mahidol University), Alan H. Beggs(Boston Children's Hospital), Fumio Takada(Scottish Rite Hospital), Nigel G. Laing(Harry Perkins Institute of Medical Research), Susan T. Iannaccone(Scottish Rite Hospital), Kathryn J. Swoboda(Massachusetts General Hospital), Carina Wallgren‐Pettersson(University of Helsinki), Huazhang Tong(Scottish Rite Hospital), Va Lip(Scottish Rite Hospital)
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