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Homozygous mutation of the 5'UTR region of the L-Ferritin gene in the hereditary hyperferritinemia cataract syndrome and its impact on the phenotype

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Description scientific article published on January 8, 2013
Author/s

author: Muriel Giansily-Blaizot  Jean-Francois Schved 

Publication date January 8, 2013
Language English
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https://haematologica.org/article/download/6640/37213

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