Sex and acquired cofactors determine phenotypes of ferroportin disease

Gastroenterology

Volumn 140, Issue 4, 2011, Pages 1199-1207.e2

  Le Lan, Caroline ^a   Mosser, Annick ^a   Ropert, Martine ^a   Detivaud, Lénaïck ^a   Loustaudratti, Véronique ^b   Vitaldurand, Denis ^c   Roget, Laurent ^d   Bardoujacquet, Edouard ^a   Turlin, Bruno ^a   David, Vronique ^a   Loral, Olivier ^a   Deugnier, Yves ^a   Brissot, Pierre ^a   Jouanolle, Anne Marie ^a  

^a PONTCHAILLOU UNIVERSITY HOSPITAL   (France)

^b LIMOGES UNIVERSITY HOSPITAL   (France)

^c Department of Neurosciences   (France)

^d GRENOBLE UNIVERSITY HOSPITAL   (France)

Author keywords

Family Study; Genetic Disease; Hemochromatosis; Iron Overload

Indexed keywords

ALANINE AMINOTRANSFERASE; CARRIER PROTEIN; FERROPORTIN; PROTEIN SLC40A1; TRANSFERRIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CLINICAL ASSESSMENT; CONTROLLED STUDY; DIAGNOSTIC IMAGING; DISEASE MARKER; FAMILY HISTORY; FEMALE; FERROPORTIN DISEASE; GENE MUTATION; GENETIC ANALYSIS; GENETIC CODE; GENOTYPE PHENOTYPE CORRELATION; HISTOPATHOLOGY; HUMAN; IRON OVERLOAD; LIVER BIOPSY; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRIORITY JOURNAL; SEX DIFFERENCE;

EID: 79953179698     PISSN: 00165085     EISSN: None     Source Type: Journal    
DOI: 10.1053/j.gastro.2010.12.049     Document Type: Article

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