Cite
HARVARD Citation
Mercier, S. et al. (2017). Expanding the spectrum of congenital myopathy linked to recessive mutations in SCN4A. Neurology. p. . [Online].
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Mercier, S. et al. (2017). Expanding the spectrum of congenital myopathy linked to recessive mutations in SCN4A. Neurology. p. . [Online].