Up a level |
Wijnberg, I D; Owczarek-Lipska, Marta; Sacchetto, R; Mascarello, F; Pascoli, F; Grunberg, W; van der Kolk J. H., ; Drögemüller, Cord (2012). A missense mutation in the skeletal muscle chloride channel 1 (CLCN1) as candidate causal mutation for congenital myotonia in a New Forest pony. Neuromuscular disorders, 22(4), pp. 361-7. Amsterdam: Elsevier 10.1016/j.nmd.2011.10.001