Characteristics of participants with self-reported hemochromatosis or iron overload at HEIRS study initial screening-Reference-Cited by-同舟云学术

Characteristics of participants with self-reported hemochromatosis or iron overload at HEIRS study initial screening

Published:2008-02 Issue:2 Volume:83 Page:126-132
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Barton James C.,Acton Ronald T.,Leiendecker-Foster Catherine,Lovato Laura,Adams Paul C.,Eckfeldt John H.,McLaren Christine E.,Reiss Jacob A.,McLaren Gordon D.,Reboussin David M.,Gordeuk Victor R.,Speechley Mark R.,Press Richard D.,Dawkins Fitzroy W.,

Publisher

Wiley

Subject

Hematology

Reference70 articles.

1. Three kinships with ALAS2 P520L (c. 1559 C → T) mutation, two in association with severe iron overload, and one with sideroblastic anemia and severe iron overload

2. Clinical expression of C282Y homozygous HFE haemochromatosis at 14 years of age

3. Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis

4. Genetic abnormalities and juvenile hemochromatosis: mutations of the HJV gene encoding hemojuvelin

5. HJV gene mutations in European patients with juvenile hemochromatosis

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