Selenoprotein N is dynamically expressed during mouse development and detected early in muscle precursors

BACKGROUND: In humans, mutations in the SEPN1 gene, encoding selenoprotein N (SelN), are involved in early onset recessive neuromuscular disorders, referred to as SEPN1-related-myopathies. The mechanisms behind these pathologies are poorly understood since the function of SelN remains elusive. Howev...

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Autors principals: Castets, Perrine, Maugenre, Svetlana, Gartioux, Corine, Rederstorff, Mathieu, Krol, Alain, Lescure, Alain, Tajbakhsh, Shahragim, Allamand, Valérie, Guicheney, Pascale
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2009
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2739516/
https://ncbi.nlm.nih.gov/pubmed/19698141
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-213X-9-46
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