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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

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

Giansily-Blaizot, M.; Cunat, S.; Moulis, G.; Schved, J.-F.; Aguilar-Martinez, P.

期刊名称Haematologica
作者Giansily-Blaizot, M.; Cunat, S.; Moulis, G.; Schved, J.-F.; Aguilar-Martinez, P.
卷第98卷
期第4期
印刷ISSN0390-6078
电子ISSN1592-8721
文件大小108.43KB
发表时间2013-04-01
DOI10.3324/haematol.2012.077198

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