Clinical, genetic, neuroimaging, and severity spectrum of peroxisomal disorders in Iran: a multicenter cohort study. Khan G S, Mashayekhi N, Bayat S, Beiraghi Toosi M, Hosseinpour S, Pak N, Dircks D, Rezaei Z, Badv R S, Zamani G, et al. Orphanet J Rare Dis. 2026 Aug 12; 21(1). PMID: 43010042. Abstract CommentRecommendBookmarkWatch