P13 Identification of a novel group of muscular dystrophies, the Anoctaminopathies, caused by recessive mutations in the putative calcium activated chloride channel, ANO5
Titel:
P13 Identification of a novel group of muscular dystrophies, the Anoctaminopathies, caused by recessive mutations in the putative calcium activated chloride channel, ANO5
Auteur:
Marlow, G. Bolduc, V. Boycott, K.M. Saleki, K. Inoue, H. Kroon, J. Itakura, M. Robitaille, Y. Parent, L. Baas, F. Mizuta, K. Kamata, N. Richard, I. Linssen, W. Mahjneh, I. de Visser, M. Brais, B. Bashir, R.