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Article

Hereditary hyperferritinemia-cataract syndrome: a novel mutation in the iron-responsive element of the L-ferritin gene in a French family.

The American journal of medicine - 15 Jul 2004

Garderet Laurent, Hermelin Brigitte, Gorin Norbert Claude, Rosmorduc Olivier

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 15234655
DOI: 10.1016/j.amjmed.2004.02.033

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Hereditary hyperferritinemia-cataract syndrome: a novel mutation in the iron-responsive element of the L-ferritin gene in a French family.PMID 15234655Read ↗

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Hereditary hyperferritinemia-cataract syndrome (HHCS) presenting with iron deficiency anemia associated with a new mutation in the iron responsive element of the L ferritin gene in a Swiss family.Semantic proximity Read ↗

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Novel ferritin L-chain gene variant in a case of hereditary hyperferritinemia-cataract syndrome without family history.Semantic proximity Read ↗

A novel double nucleotide variant in the ferritin-L iron-responsive element in a Finnish patient with hereditary hyperferritinaemia-cataract syndrome.Semantic proximity Read ↗

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Hereditary hyperferritinemia-cataract syndrome: relationship between phenotypes and specific mutations in the iron-responsive element of ferritin light-chain mRNA.Semantic proximity Read ↗

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