SAXS curve of human ferritin pathogenic mutant LN2 (DNA mutation c.497_498dupTC, causing the amino acid change p.Phe167SerfsX26) with 50 Iron/protein shell

SAXS curve of human ferritin mutant LN2, associated with the neurodegenerative disorder neuroferritinopathy (MeSH term: C548080; Orphanet classification: Disorder; ICD-11 code: 8A01.1Y – chorea due to neuroferritinopathy), loaded with 50 Iron/protein shell, corresponding to 3 Iron/Ferritin monomer.