Literature DB >> 9882097

Coinheritance of alleles associated with hemochromatosis and hereditary hyperferritinemia-cataract syndrome.

J C Barton, E Beutler, T Gelbart.   

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Year:  1998        PMID： 9882097

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  5 in total

Review 1.  Recent advance in molecular iron metabolism: translational disorders of ferritin.

Authors:  Junji Kato; Yoshiro Niitsu
Journal:  Int J Hematol       Date:  2002-10       Impact factor: 2.490

2.  Characteristics of participants with self-reported hemochromatosis or iron overload at HEIRS study initial screening.

Authors:  James C Barton; Ronald T Acton; Catherine Leiendecker-Foster; Laura Lovato; Paul C Adams; John H Eckfeldt; Christine E McLaren; Jacob A Reiss; Gordon D McLaren; David M Reboussin; Victor R Gordeuk; Mark R Speechley; Richard D Press; Fitzroy W Dawkins
Journal:  Am J Hematol       Date:  2008-02       Impact factor: 10.047

Review 3.  Hyperferritinaemia-cataract syndrome: worldwide mutations and phenotype of an increasingly diagnosed genetic disorder.

Authors:  Gunda Millonig; Martina U Muckenthaler; Sebastian Mueller
Journal:  Hum Genomics       Date:  2010-04       Impact factor: 4.639

4.  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

5.  Hereditary Hyperferritinemia-Cataract Syndrome in 3 Generations of a Family in East Tennessee.

Authors:  Heidi A Worth; Zachary Marlette; David Aljadir; Ronald Lands
Journal:  Case Rep Hematol       Date:  2020-05-26
  5 in total

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