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Case Reports
. 1996 Sep 1;88(5):1895.

A novel mutation in the iron responsive element of ferritin L-subunit gene as a cause for hereditary hyperferritinemia-cataract syndrome

  • PMID: 8781450
Free article
Case Reports

A novel mutation in the iron responsive element of ferritin L-subunit gene as a cause for hereditary hyperferritinemia-cataract syndrome

P Aguilar-Martinez et al. Blood. .
Free article
No abstract available

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