Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy

Marian A. J. Weterman, Marian A. J. Weterman, Marian A. J. Weterman, Peter G. Barth, Peter G. Barth, Peter G. Barth, Karin Y. van Spaendonck-Zwarts, Karin Y. van Spaendonck-Zwarts, Karin Y. van Spaendonck-Zwarts, Eleonora Aronica, Eleonora Aronica, Eleonora Aronica, Bwee-Tien Poll-The, Bwee-Tien Poll-The, Bwee-Tien Poll-The, Oebele F. Brouwer, Oebele F. Brouwer, Oebele F. Brouwer, J. Peter van Tintelen, J. Peter van Tintelen, J. Peter van Tintelen, Zohal Qahar, Zohal Qahar, Zohal Qahar, Edward J. Bradley, Edward J. Bradley, Edward J. Bradley, Marit de Wissel, Marit de Wissel, Marit de Wissel, Leonardo Salviati, Leonardo Salviati, Leonardo Salviati, Corrado Angelini, Corrado Angelini, Corrado Angelini, Lambertus van den Heuvel, Lambertus van den Heuvel, Lambertus van den Heuvel, Yolande E. M. Thomasse, Yolande E. M. Thomasse, Yolande E. M. Thomasse, Ad P. Backx, Ad P. Backx, Ad P. Backx, Gudrun Nürnberg, Gudrun Nürnberg, Gudrun Nürnberg, Peter Nürnberg, Peter Nürnberg, Peter Nürnberg, Frank Baas, Frank Baas, Frank Baas
  • Brain, January 2013, Oxford University Press (OUP)
  • DOI: 10.1093/brain/aws293

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http://dx.doi.org/10.1093/brain/aws293

The following have contributed to this page: Prof Corrado Angelini