Selenoprotein N deficiency in mice is associated with abnormal lung development

Mutations in the human SEPN1 gene, encoding selenoprotein N (SepN), cause SEPN1-related myopathy (SEPN1-RM) characterized by muscle weakness, spinal rigidity, and respiratory insufficiency. As with other members of the selenoprotein family, selenoprotein N incorporates selenium in the form of seleno...

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Detalhes bibliográficos
Main Authors: Moghadaszadeh, Behzad, Rider, Branden E., Lawlor, Michael W., Childers, Martin K., Grange, Robert W., Gupta, Kushagra, Boukedes, Steve S., Owen, Caroline A., Beggs, Alan H.
Formato: Artigo
Idioma:Inglês
Publicado em: Federation of American Societies for Experimental Biology 2013
Assuntos:
Research Communications
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3606527/
https://ncbi.nlm.nih.gov/pubmed/23325319
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1096/fj.12-212688
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