A Q312X mutation in the hemojuvelin gene is associated with cardiomyopathy due to juvenile haemochromatosis☆-Reference-Cited by-同舟云学术

A Q312X mutation in the hemojuvelin gene is associated with cardiomyopathy due to juvenile haemochromatosis☆

Published:2008-10 Issue:10 Volume:10 Page:1001-1006
ISSN:1388-9842
Container-title:European Journal of Heart Failure
language:en
Short-container-title:European Journal of Heart Failure

Author:

Nagayoshi Yasuhiro¹,Nakayama Masafumi¹,Suzuki Satoru¹,Hokamaki Jun¹,Shimomura Hideki¹,Tsujita Kenichi¹,Fukuda Masaya¹,Yamashita Takuro¹,Nakamura Yoshinori¹,Sugiyama Seigo¹,Ogawa Hisao¹

Affiliation:

1. Department of Cardiovascular Medicine; Graduate School of Medical Sciences, Kumamoto University; Kumamoto City Japan

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

Reference30 articles.

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4. Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators. Hemochromatosis and iron-overload screening in a racially diverse population;Adams;N Engl J Med,2005

5. Juvenile hemochromatosis;Kaltwasser,2000

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