A missense mutation in the skeletal muscle chloride channel 1 (CLCN1) as candidate causal mutation for congenital myotonia in a New Forest pony

I.D. Wijnberg, M. Owczarek-Lipska, R. Sacchetto, F. Mascarello, F. Pascoli, W. Gruenberg, J.H. van der Kolk, C. Drögemüller

    Research output: Contribution to journalArticleAcademicpeer-review

    Original languageUndefined/Unknown
    Pages (from-to)361-367
    Number of pages7
    JournalNeuromuscular Disorders
    Volume22
    Publication statusPublished - 2012

    Cite this