Original language | English |
---|---|
Pages (from-to) | 494-507 |
Journal | Brain |
Volume | 136 |
DOIs | |
Publication status | Published - 2013 |
K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity
N. Mokbel, B. Ilkovski, M. Kreissl, M. Memo, C.M. Jeffries, M. Marttila, V.-L. Lehtokari, E. Lemola, M. Grönholm, N. Yang, D. Menard, P. Marcorelles, A. Echaniz-Laguna, J. Reimann, M. Vainzof, N. Monnier, Gina Ravenscroft, Elyshia McNamara, Kristen Nowak, Nigel Laing
Research output: Contribution to journal › Article › peer-review
43
Citations
(Scopus)