Items where Author is "Kuntzer, T."
Jump to: 2009 Number of items: 2. 2009Huze, C. and Bauche, S. and Richard, P. and Chevessier, F. and Goillot, E. and Gaudon, K. and Ben Ammar, A. and Chaboud, A. and Grosjean, I. and Lecuyer, H. -A. and Bernard, V. and Rouche, A. and Alexandri, N. and Kuntzer, T. and Fardeau, M. and Fournier, E. and Brancaccio, A. and Ruegg, M. A. and Koenig, J. and Eymard, B. and Schaeffer, L. and Hantai, D.. (2009) Identification of an agrin mutation that causes congenital myasthenia and affects synapse function. American Journal of Human Genetics, 85 (2). pp. 155-167. Lalive, P. H. and Passweg, J. R. and Kuntzer, T.. (2009) [Neuropathy associated with monoclonal gammopathy (dysglobulinemia)]. Revue médicale suisse : revue officielle de la Société médicale de la Suisse romande ... [et al.], Vol. 5 , S. 962-4, 966-967. |