Literature DB >> 21210779

Identification of the mutations associated with hereditary hyperferritinemia cataract syndrome and hemochromatosis in a Brazilian family.

F G A Meneses, B Schnabel, I D C G Silva, F L Alberto, L Toma, H B Nader, C C Lopes.   

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Year:  2011        PMID： 21210779     DOI： 10.1111/j.1399-0004.2010.01517.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  1 in total

1.  Ferritin light chain gene mutations in two Brazilian families with hereditary hyperferritinemia-cataract syndrome.

Authors:  Roberta Cardoso Petroni; Susana Elaine Alves da Rosa; Flavia Pereira de Carvalho; Rúbia Anita Ferraz Santana; Joyce Esteves Hyppolito; Claudia Mac Donald Bley Nascimento; Nelson Hamerschlak; Paulo Vidal Campregher
Journal:  Einstein (Sao Paulo)       Date:  2017-07-24
  1 in total

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