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Elsevier, Neuromuscular Disorders, 1(31), p. 21-28, 2021

DOI: 10.1016/j.nmd.2020.10.006

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Presynaptic congenital myasthenic syndrome due to three novel mutations in SLC5A7 encoding the sodium-dependant high-affinity choline transporter

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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