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HARVARD Citation
Chang, T. et al. (2016). A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case report. BMC neurology. 16 (1), pp. 1-4. [Online].
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Chang, T. et al. (2016). A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case report. BMC neurology. 16 (1), pp. 1-4. [Online].