Literature DB >> 19372266

Homozygous deletion of HFE: the Sardinian hemochromatosis?

Sara Pelucchi, Raffaella Mariani, Francesca Bertola, Cristina Arosio, Alberto Piperno.   

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Year:  2009        PMID： 19372266     DOI： 10.1182/blood-2008-12-196493

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


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  3 in total

1.  Homozygous deletion of HFE is the common cause of hemochromatosis in Sardinia.

Authors:  Gérald Le Gac; Rita Congiu; Isabelle Gourlaouen; Milena Cau; Claude Férec; Maria Antonietta Melis
Journal:  Haematologica       Date:  2009-12-08       Impact factor: 9.941

Review 2.  Molecular diagnostic and pathogenesis of hereditary hemochromatosis.

Authors:  Paulo C J L Santos; Jose E Krieger; Alexandre C Pereira
Journal:  Int J Mol Sci       Date:  2012-02-01       Impact factor: 6.208

Review 3.  Pathophysiological consequences and benefits of HFE mutations: 20 years of research.

Authors:  Ina Hollerer; André Bachmann; Martina U Muckenthaler
Journal:  Haematologica       Date:  2017-03-09       Impact factor: 9.941
  3 in total

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