G80S-linked ferroportin disease: The first clinical description in a Greek family

Blood Cells, Molecules, and Diseases

Volumn 41, Issue 1, 2008, Pages 138-139

  Mougiou, A ^a   Pietrangelo, A ^b   Caleffi, A ^b   Kourakli, A ^a   Karakantza, M ^a   Zoumbos, N ^a  

^a UNIVERSITY OF PATRAS   (Greece)

^b UNIVERSITY OF MODENA AND REGGIO EMILIA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

FERROPORTIN; NUCLEOTIDE;

ADULT; AGED; ANEMIA; AUTOSOMAL DOMINANT INHERITANCE; BODY WEIGHT; CASE REPORT; CATARACT; CLINICAL FEATURE; DISEASE COURSE; DISEASE SEVERITY; EXON; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC DISORDER; GENETIC MARKER; GREECE; HEMOSIDEROSIS; HUMAN; IRON OVERLOAD; LABORATORY TEST; LETTER; MISSENSE MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PHLEBOTOMY; PRIORITY JOURNAL;

ADULT; AGED, 80 AND OVER; CATION TRANSPORT PROTEINS; EXONS; FAMILY; FERRITINS; GREECE; HEMOCHROMATOSIS; HUMANS; IRON OVERLOAD; MALE; MUTATION, MISSENSE; PHLEBOTOMY; TRANSFERRIN;

EID: 44449113578     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcmd.2008.03.002     Document Type: Letter

References (8)

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