Letters to the Editor

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

Laboratory of Hematology, Hôpital Saint Eloi, CHU of Montpellier, France
Laboratory of Hematology, Hôpital Saint Eloi, CHU of Montpellier, France
Laboratory of Hematology, Hôpital Saint Eloi, CHU of Montpellier, France
Laboratory of Hematology, Hôpital Saint Eloi, CHU of Montpellier, France
Laboratory of Hematology, Hôpital Saint Eloi, CHU of Montpellier, France
Vol. 98 No. 4 (2013): April, 2013 https://doi.org/10.3324/haematol.2012.077198