A homozygous HFE gene splice site mutation (IVS5+1 G/A) in a hereditary hemochromatosis patient of Vietnamese origin

Gastroenterology

Volumn 122, Issue 3, 2002, Pages 789-795

  Steiner, Michael ^a   Ocran, Kenneth ^b   Genschel, Janine ^b   Meier, Patrick ^a   Gerl, Helga ^b   Ventz, Michael ^b   Schneider, Marie Luise ^b   Büttner, Carsten ^b   Wadowska, Kamilla ^a   Kerner, Wolfgang ^a   SchuffWerner, Peter ^a   Lochs, Herbert ^a,b   Schmidt, Hartmut ^a,b  

^a UNIVERSITY OF ROSTOCK   (Germany)

^b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

FERRITIN; IRON; TRANSFERRIN;

ADRENAL CORTEX INSUFFICIENCY; ADULT; ALLELE; ARTICLE; CASE REPORT; CAUCASIAN; EXON; GENE MUTATION; GENETIC DISORDER; HEMOCHROMATOSIS; HOMOZYGOSITY; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; INTRON; IRON BLOOD LEVEL; MALE; MISSENSE MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RNA SPLICING; VIET NAM;

EID: 0036177789     PISSN: 00165085     EISSN: None     Source Type: Journal    
DOI: 10.1053/gast.2002.31884     Document Type: Article

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