Original language | English |
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Pages (from-to) | 613-617 |
Journal | Neurology |
Volume | 59 |
Publication status | Published - 2002 |
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 journal › Article › peer-review
70
Citations
(Scopus)