Ferroportin-related haemochromatosis associated with novel Y64H mutation of the SCL40A1 gene

Przeglad Gastroenterologiczny

Volumn 9, Issue 5, 2014, Pages 307-309

  Raszeja Wyszomirska, Joanna ^a   Caleffi, Angela ^b   Milkiewicz, Piotr ^a   Pietrangelo, Antonello ^b  

^a MEDICAL UNIVERSITY OF WARSAW   (Poland)

^b UNIVERSITY OF MODENA AND REGGIO EMILIA   (Italy)

Author keywords

c.190T>C mutation; Ferroportin disease; Haemochromatosis; Liver cirrhosis; Non classical form

Indexed keywords

FERROPORTIN;

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; DATA BASE; EPIGASTRIC PAIN; EXON; FATIGUE; GENE; GENE MUTATION; GENETIC TRAIT; HEMOCHROMATOSIS; HUMAN; HUMAN TISSUE; INHERITANCE; IRON OVERLOAD; LIVER FIBROSIS; MALE; MENDELIAN RANDOMIZATION ANALYSIS; PHENOTYPE; SCL40A1 GENE; WEAKNESS;

EID: 84908292640     PISSN: 18955770     EISSN: 18974317     Source Type: Journal    
DOI: 10.5114/pg.2014.46167     Document Type: Article

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