Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms. Issue 6 (1st June 2004)

• Record Type: Journal Article
• Authors: Cremonesi, L; Cozzi, A; Girelli, D; Ferrari, F; Fermo, I; Foglieni, B; Levi, S; Bozzini, C; Camparini, M; Ferrari, M; Arosio, P
• Is Part Of: Journal of medical genetics. Volume 41:Issue 6(2004)
• Page Start: e81
• Page End: e81
• Publication Date: 2004-06-01
• Subjects: hyperferritinaemia -- iron metabolism -- iron responsive element -- neurodegenerative disorders -- neuroferritinopathy; HHCS, hyperferritinaemia cataract syndrome -- IRE, iron responsive element -- IRP, iron regulatory protein; Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmg.2003.011718
• Languages: English
• ISSNs: 1468-6244