This scientific commentary refers to “Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or ‘classical’ congenital myopathy”, by Zaharieva et al. (doi:10.1093/brain/awv352).
CITATION STYLE
Cannon, S. C. (2016). When all is lost…a severe myopathy with hypotonia from sodium channel mutations. Brain, 139(3), 642–644. https://doi.org/10.1093/brain/awv400
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