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HARVARD Citation
Müller, J. et al. (2004). The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder. Journal of medical genetics. 41 (8), p. e104. [Online].
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Müller, J. et al. (2004). The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder. Journal of medical genetics. 41 (8), p. e104. [Online].