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A missense mutation in the skeletal muscle chloride channel 1 (CLCN1) as candidate causal mutation for congenital myotonia in a New Forest pony
Inge D. Wijnberg, Marta Owczarek-Lipska, Roberta Sacchetto, Francesco Mascarello, Francesco Pascoli, Walter Grünberg, Johannes H. van der Kolk, Cord DrögemüllerVolume:
22
Year:
2012
Language:
english
DOI:
10.1016/j.nmd.2011.10.001
File:
PDF, 1.14 MB
english, 2012