G.P.270 von Lehtokari, V.L, Kiiski, K, Pelin, K, Wallgren-Pettersson, C

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G.P.266 von Kiiski, K, Lehtokari, V.L, Laari, L, Wallgren-Pettersson, C, Pelin, K

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P.9.8 Nemaline myopathy: Mutations in alternatively spliced exons of the nebulin gene von Lehtokari, V.L, Laitila, J, Hanif, M, Pelin, K, Wallgren-Pettersson, C

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G.P.9.04 Development of the multiplex ligation-dependent probe amplification (MLPA) method for identifying large scale mutations in the nebulin gene von Lunkka-Hytonen, M, Lehtokari, V.L, Pelin, K, Brudzewsky, D, Wallgren-Pettersson, C

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G.P.9.03 Characterization of the nebulin promoter and detection of brain-specific transcripts von Ranta, S.A, Lehtokari, V.L, Nuutinen, E, Brudzewsky, D, Wallgren-Pettersson, C, Pelin, K

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G.P.270: A large genomic rearrangement affecting TPM3 causing severe nemaline myopathy von Lehtokari, V.L., Kiiski, K., Pelin, K., Wallgren-Pettersson, C.

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G.P.274: Cold shock domain protein A – A novel nemaline myopathy-causing gene? von Laitila, J., Lehtokari, V.L., Kiiski, K., Wallgren-Pettersson, C., Pelin, K.

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G.P.266: Large copy number variations in NEB are frequent in nemaline myopathy patients von Kiiski, K., Lehtokari, V.L., Laari, L., Wallgren-Pettersson, C., Pelin, K.

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G.P.271: Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies von Marttila, M., Lehtokari, V.L., Marston, S.B., Nyman, T.A., Barnerias, C., Beggs, A.H., Bertin, E., Ceyhan-Birsoy, Ö., Cintas, P., Gerard, M., Gilbert-Dussardier, B., Hogue, J.S., Longman, C., Eymard, B., Frydman, M., Kang, P.B., Klinge, L., Kolski, H., Lochmüller, H., Magy, L., Manel, V., Mayer, M., North, K.N., Peudenier-Robert, S., Pihko, H., Probst, F.J., Reisin, R., Stewart, W., Taratuto, A.L., de Visser, M., Wilichowski, E., Winer, J., Nowak, K., Lain, N.G., Winder, T.L., Monnier, N., Clarke, N.F., Pelin, K., Grönholm, M., Wallgren-Pettersson, C.

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G.P.8 01 Development of the multiplex ligation-dependent probe amplification (MLPA) method for the detection of large deletions in the nebulin gene von Lehtokari, V.L., Pelin, K., Nuutinen, E., Wallgren-Pettersson, C.

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