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24. Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2). Tajsharghi H; Ohlsson M; Lindberg C; Oldfors A Arch Neurol; 2007 Sep; 64(9):1334-8. PubMed ID: 17846275 [TBL] [Abstract][Full Text] [Related]
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