A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload

American Journal of Human Genetics

Volumn 69, Issue 1, 2001, Pages 191-197

  Kato, Junji ^a   Fujikawa, Koshi ^a   Kanda, Megumi ^a,b   Fukuda, Nao ^a,b   Sasaki, Katsunori ^a   Takayama, Tetsuji ^a   Kobune, Masayoshi ^a   Takada, Kohichi ^a   Takimoto, Rishu ^a   Hamada, Hirofumi ^a   Ikeda, Tatsuru ^c   Niitsu, Yoshiro ^a  

^a SAPPORO MEDICAL UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b SAPPORO MEDICAL UNIVERSITY HOSPITAL   (Japan)

^c HOKKAIDO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CERULOPLASMIN; FERRITIN; IRON; IRON REGULATORY FACTOR; MESSENGER RNA; PROTEIN SUBUNIT;

ANIMAL CELL; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BINDING AFFINITY; ENZYME ACTIVITY; GENE MUTATION; HEMOCHROMATOSIS; IRON OVERLOAD; IRON RESPONSIVE ELEMENT; IRON STORAGE; IRON TRANSPORT; ISOTOPE LABELING; NONHUMAN; POINT MUTATION; PRIORITY JOURNAL; SCATCHARD PLOT; SYNTHESIS;

EID: 0034964604     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/321261     Document Type: Article

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