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Mutation Update and Genotype-Phenotype Correlations of Novel and Previously Described Mutations in TPM2 and TPM3 Causing Congenital Myopathies

  • M. Marttila
  • , V.L. Lehtokari
  • , S.B. Marston
  • , T.A. Nyman
  • , C. Barnérias
  • , A.H. Beggs
  • , E. Bertini
  • , O. Ceyhan-Birsoy
  • , P. Cintas
  • , M.J. Gérard
  • , B. Gilbert-Dussardier
  • , J.S. Hogue
  • , C.A.L. Longman
  • , B. Eymard
  • , M.I. Frydman
  • , P. Kang
  • , L. Klinge
  • , H.K. Kolski
  • , H. Lochmüller
  • , L. Magy
    • V. Manel, M.N. Mayer, E.A. Mercuri, K.N. North, S. Peudenier-Robert, H. Pihko, F.J. Probst, R.C. Reisin, W.R. Stewart, A.L. Taratuto, M. De Visser, E.K.G. Wilichowski, J.B. Winer, Kristen Nowak, Nigel Laing, T.L. Winder, N. Monnier, N.F. Clarke, K. Pelin, M. Grönholm, C. Wallgren-Pettersson

Research output: Contribution to journal › Article › peer-review

102   Link opens in a new tab Citations (Scopus)

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