The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder

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Bibliographic Details
Main Authors:	Muller, J, Abicht, A, Burke, G, Cossins, J, Richard, P, Baumeister, S, Stucka, R, Eymard, B, Hantai, D, Beeson, D, Lochmuller, H
Format:	Artigo
Language:	Inglês
Published:	BMJ Group 2004
Subjects:	Electronic Letter
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC1735862/ https://ncbi.nlm.nih.gov/pubmed/15286164 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.021139
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