Cite
HARVARD Citation
Finlayson, S. et al. (2013). Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1. Journal of neurology, neurosurgery and psychiatry. 84 (10), pp. 1119-1125. [Online].
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Finlayson, S. et al. (2013). Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1. Journal of neurology, neurosurgery and psychiatry. 84 (10), pp. 1119-1125. [Online].