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 LaingC. Wallgren-Pettersson, J. Trewhella, S. Marston, C. Ottenheijm, K.N. North, N.F. Clarke

Research output: Contribution to journalArticlepeer-review

43 Citations (Scopus)
Original languageEnglish
Pages (from-to)494-507
JournalBrain
Volume136
DOIs
Publication statusPublished - 2013

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