Lens changes in hereditary hyperferritinemia-cataract syndrome
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference6 articles.
1. Bilateral cataract and high serum ferritin;Bonneau;J Med Genet,1995
2. A linkage between hereditary hyperferritinemia not related to iron overload and autosomal dominant congenital cataract;Girelli;Br J Haematol,1995
3. Hereditary hyperferritinemia-cataract syndrome;Cazzola;Blood,1997
4. Mutation in the iron responsive element of L-ferritin mRNA in a family with dominant hyperferritinemia and cataract;Beaumont;Nature Genet,1995
5. Clinical severity and thermodynamic effects of iron-responsive element mutations in hereditary hereditary hyperferritinemia-cataract syndrome;Allerson;J Biol Chem,1999
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1. Genotypic–Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian Families;International Journal of Molecular Sciences;2023-07-25
2. Duet procedure to achieve reversible trifocality in a young patient with hereditary hyperferritinemia-cataract syndrome;American Journal of Ophthalmology Case Reports;2021-03
3. Ferritin L-subunit gene mutation and hereditary hyperferritinaemia cataract syndrome (HHCS): a case report and literature review;Hematology;2021-01-01
4. Hyperferritinemia-cataract syndrome: Long-term ophthalmic observations in an Italian family;Ophthalmic Genetics;2016-02-05
5. Homozygous mutation of the 5'UTR region of the L-Ferritin gene in the hereditary hyperferritinemia cataract syndrome and its impact on the phenotype;Haematologica;2013-01-08
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