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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.

ABSTRACT:

SUBMITTER: Giansily-Blaizot M 

PROVIDER: S-EPMC3660001 | biostudies-literature | 2013 Apr

REPOSITORIES: biostudies-literature

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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.

Giansily-Blaizot Muriel M   Cunat Séverine S   Moulis Grégory G   Schved Jean-François JF   Aguilar-Martinez Patricia P  

Haematologica 20130108 4

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