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A single homozygous point mutation in a 3′untranslated region motif of selenoprotein N mRNA causes SEPN1-related myopathy

✍ Scribed by Allamand, Valérie; Richard, Pascale; Lescure, Alain; Ledeuil, Céline; Desjardin, Delphine; Petit, Nathalie; Gartioux, Corine; Ferreiro, Ana; Krol, Alain; Pellegrini, Nadine; Urtizberea, J Andoni; Guicheney, Pascale

Book ID: 110032997
Publisher: Nature Publishing Group
Year: 2006
Tongue: English
Weight: 130 KB
Volume: 7
Category: Article
ISSN: 1469-221X
DOI: 10.1038/sj.embor.7400648

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