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Article

Selenoprotein N deficiency in mice is associated with abnormal lung development.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology - 1 Apr 2013

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

Abstract excerpt

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 sel...

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Identifiers

PMID: 23325319
DOI: 10.1096/fj.12-212688
PMCID: PMC3606527

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-23325319-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

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