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HARVARD Citation
O'Grady, G. et al. (2016). Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome. Neurology. p. . [Online].
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O'Grady, G. et al. (2016). Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome. Neurology. p. . [Online].