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Screening of mutations in NOL3 in a myoclonic syndromes series

Detalles Bibliográficos
Autores principales:	Macerollo, A., Mencacci, N. E., Erro, R., Cordivari, C., Edwards, M. J., Wood, N. W., Bhatia, Kailash P.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Berlin Heidelberg 2014
Materias:	Letter to the Editors
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155162/ https://www.ncbi.nlm.nih.gov/pubmed/25138476 http://dx.doi.org/10.1007/s00415-014-7463-z

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