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Severe congenital myasthenic syndrome due to homozygosity of the 1293insG -acetylcholine receptor subunit mutation.

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http://pubman.mpdl.mpg.de/cone/persons/resource/persons80526

Sieb,  J. P.
Max Planck Institute of Psychiatry, Max Planck Society;

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Sieb, J. P., Kraner, S., Schrank, B., Reitter, B., Goebel, T. H. H., Tzartos, S. J., et al. (2000). Severe congenital myasthenic syndrome due to homozygosity of the 1293insG -acetylcholine receptor subunit mutation. Annals of Neurology, 48, 379-383.


Cite as: http://hdl.handle.net/11858/00-001M-0000-000E-A576-3
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