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4. [Hyperferritinemia-cataract syndrome associated to the HFE gene mutation. Two new Spanish families and a new mutation (A37T: "Zaragoza")]. García Erce JA; Cortés T; Cremonesi L; Cazzola M; Pérez-Lungmus G; Giralt M Med Clin (Barc); 2006 Jun; 127(2):55-8. PubMed ID: 16900584 [TBL] [Abstract][Full Text] [Related]
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10. Hereditary hyperferritinemia-cataract syndrome: relationship between phenotypes and specific mutations in the iron-responsive element of ferritin light-chain mRNA. Cazzola M; Bergamaschi G; Tonon L; Arbustini E; Grasso M; Vercesi E; Barosi G; Bianchi PE; Cairo G; Arosio P Blood; 1997 Jul; 90(2):814-21. PubMed ID: 9226182 [TBL] [Abstract][Full Text] [Related]
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12. Hereditary hyperferritinemia cataract syndrome as a cause of childhood hyperferritinemia. Tsantoula F; Kioumi A; Germenis AE; Speletas M J Pediatr Hematol Oncol; 2014 Jul; 36(5):e304-6. PubMed ID: 24983587 [TBL] [Abstract][Full Text] [Related]
13. Description of a new mutation in the L-ferrin iron-responsive element associated with hereditary hyperferritinemia-cataract syndrome in a Spanish family. Balas A; Aviles MJ; Garcia-Sanchez F; Vicario JL Blood; 1999 Jun; 93(11):4020-1. PubMed ID: 10383191 [No Abstract] [Full Text] [Related]
14. Hereditary hyperferritinemia cataract syndrome: clinical, genetic, and laboratory findings in 5 families. Nonnenmacher L; Langer T; Blessing H; Gabriel H; Buchwald HJ; Meneksedag C; Kohne E; Gencik M; Debatin KM; Cario H Klin Padiatr; 2011 Nov; 223(6):346-51. PubMed ID: 22020773 [TBL] [Abstract][Full Text] [Related]
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18. FTL c.-168G>C Mutation in Hereditary Hyperferritinemia Cataract Syndrome: A New Italian Family. Ferro E; Capra AP; Zirilli G; Meduri A; Urso M; Briuglia S; La Rosa MA Pediatr Dev Pathol; 2018; 21(5):456-460. PubMed ID: 29426274 [TBL] [Abstract][Full Text] [Related]
19. Ferritin crystal cataracts in hereditary hyperferritinemia cataract syndrome. Brooks DG; Manova-Todorova K; Farmer J; Lobmayr L; Wilson RB; Eagle RC; St Pierre TG; Stambolian D Invest Ophthalmol Vis Sci; 2002 Apr; 43(4):1121-6. PubMed ID: 11923255 [TBL] [Abstract][Full Text] [Related]
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