Mattila RM, Sainio A, Järveläinen M, Pursiheimo J, Järveläinen H. A novel double nucleotide variant in the ferritin-L iron-responsive element in a Finnish patient with hereditary hyperferritinaemia-cataract syndrome. Acta Ophthalmol. 2018 Feb;96(1):95–9. doi: 10.1111/aos.13492. PMID: 28636169.