Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

Blood

Volumn 100, Issue 2, 2002, Pages 692-694

  Wallace, Daniel F ^a,b,c   Pedersen, Palle ^a,b,c   Dixon, Jeannette L ^a,b,c   Stephenson, Peter ^a,b,c   Searle, Jeffrey W ^a,b,c   Powell, Lawrie W ^a,b,c   Subramaniam, V Nathan ^a,b,c,d  

^a ROYAL BRISBANE AND WOMEN'S HOSPITAL   (Australia)

^b UNIVERSITY OF QUEENSLAND   (Australia)

^c NAESTVED HOSPITAL   (Denmark)

^d QIMR BERGHOFER MEDICAL RESEARCH INSTITUTE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

IRON; TRANSFERRIN RECEPTOR;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CONTROLLED STUDY; FERROPORTIN1 GENE; GENE MUTATION; HEMOCHROMATOSIS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IRON KINETICS; LIVER BIOPSY; MALE; PATHOPHYSIOLOGY; PRIORITY JOURNAL;

EID: 0037100517     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.V100.2.692     Document Type: Article

References (19)

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