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, Nigel Laing, A.H. Beggs

Research output: Contribution to journalArticle

70 Citations (Scopus)
Original languageEnglish
Pages (from-to)613-617
JournalNeurology
Volume59
Publication statusPublished - 2002

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