The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder.
Müller, J. S.; Abicht, A.; Burke, G.; Cossins, J.; Richard, P.; Baumeister, S. K.; Stucka, R.; Eymard, B.; Hantaï, D.; Beeson, D.; Lochmüller, H.; Journal of Medical Genetics, 2004, vol. 41, issue 8, p e104, ISSN 00222593. ISBN 14686244.

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