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Article

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

Haematologica - 1 Apr 2013

Giansily-Blaizot Muriel, Cunat Séverine, Moulis Grégory, Schved Jean-François, Aguilar-Martinez Patricia

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Share to 5' Untranslated Regions
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 23300176
DOI: 10.3324/haematol.2012.077198
PMCID: PMC3660001

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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.PMID 23300176Read ↗

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