Browsing by Author Lehtokari, V-L
Showing results 1 to 1 of 1
| Issue Date | Title | Author(s) |
| 15-Nov-2012 | K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity | Mokbel, N; Ilkovski, B; Kreissl, M; Memo, M; Jeffries, CM; Marttila, M; Lehtokari, V-L; Lemola, E; Grönholm, M; Yang, N; Menard, D; Marcorelles, P; Echaniz-Laguna, A; Reimann, J; Vainzof, M; Monnier, N; Ravenscroft, G; McNamara, E; Nowak, KJ; Laing, NG; Wallgren-Pettersson, C; Trewhella, J; Marston, S; Ottenheijm, C; North, KN; Clarke, NF |
