Literature DB >> 12150153

Mutation analysis of transferrin-receptor 2 in patients with atypical hemochromatosis.

Wolf-K Hofmann, Xiang-Jun Tong, Richard S Ajioka, James P Kushner, H Phillip Koeffler.   

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Year:  2002        PMID： 12150153     DOI： 10.1182/blood-2002-04-1077

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


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  5 in total

Review 1.  Factors influencing disease phenotype and penetrance in HFE haemochromatosis.

Authors:  J Rochette; G Le Gac; K Lassoued; C Férec; K J H Robson
Journal:  Hum Genet       Date:  2010-07-06       Impact factor: 4.132

Review 2.  Non-HFE hemochromatosis: genetics, pathogenesis, and clinical management.

Authors:  James E Nelson; Kris V Kowdley
Journal:  Curr Gastroenterol Rep       Date:  2005-02

3.  A novel rat model of hereditary hemochromatosis due to a mutation in transferrin receptor 2.

Authors:  Thomas B Bartnikas; Sheryl J Wildt; Amy E Wineinger; Klaus Schmitz-Abe; Kyriacos Markianos; Dale M Cooper; Mark D Fleming
Journal:  Comp Med       Date:  2013-04       Impact factor: 0.982

Review 4.  Recent advances in understanding haemochromatosis: a transition state.

Authors:  K J H Robson; A T Merryweather-Clarke; E Cadet; V Viprakasit; M G Zaahl; J J Pointon; D J Weatherall; J Rochette
Journal:  J Med Genet       Date:  2004-10       Impact factor: 6.318

5.  Identification of Novel Mutations by Targeted NGS Panel in Patients with Hyperferritinemia.

Authors:  Giulia Ravasi; Sara Pelucchi; Francesca Bertola; Martina Maria Capelletti; Raffaella Mariani; Alberto Piperno
Journal:  Genes (Basel)       Date:  2021-11-09       Impact factor: 4.096
  5 in total

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