The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder.
Autors principals: | Müller, J, Abicht, A, Burke, G, Cossins, J, Richard, P, Baumeister, S, Stucka, R, Eymard, B, Hantaï, D, Beeson, D, Lochmüller, H |
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Format: | Journal article |
Idioma: | English |
Publicat: |
2004
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