S-EPMC3660001 - Homozygous mutation of the 5'UTR region of the L-Ferritin gene in the hereditary hyperferritinemia cataract syndrome and its impact on the phenotype. - OmicsDI

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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