IDENTIFICATION OF THE MOLECULAR MECHANISMS INVOLVED IN THE PATHOGENESIS OF THE HEREDITARY HYPERFERRITINEMIA-CATARACT SYNDROME
- 1 Anni 1997/1998
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Pubblicazioni Scientifiche
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Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron responsive element of ferritin L-subunit gene
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Analysis of ferritins in lymphoblastoid cell lines and in the lens of subjects with hereditary hyperferritinemia-cataract syndrome