| Literature DB >> 15897636 |
Weidong Liu1, Souji Shimomura, Hiroyasu Imanishi, Yuna Iwamoto, Naoto Ikeda, Masaki Saito, Masao Ohno, Naoki Hara, Tetsuo Yamamoto, Hideji Nakamura, Toshikazu Hada.
Abstract
The HFE, H ferritin, TFR2, and ferroportin 1 genes of a Japanese patient diagnosed as having hemochromatosis were amplified by PCR and sequenced. A novel mutation in the ferroportin 1 was found in the patient. It was located in the noncoding region of the ferroportin 1; nucleotide 117 adenine was changed to guanine, 7 nucleotides downstream the iron responsive element (IRE) region. This mutation was not found in the patient's son or daughter, or in 50 healthy individuals. It was suggested that the mutation in the ferroportin 1 may be related to hemochromatosis of this patient.Entities:
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Year: 2005 PMID: 15897636 DOI: 10.2169/internalmedicine.44.285
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271