Congenital and Familial Iron Overload-Reference-Cited by-同舟云学术

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Congenital and Familial Iron Overload

Published:1969-03-20 Issue:12 Volume:280 Page:642-645
ISSN:0028-4793
Container-title:New England Journal of Medicine
language:en
Short-container-title:N Engl J Med

Author:

Vitale L.,Opitz J. M.,Shahidi N. T.

Publisher

Massachusetts Medical Society

Subject

General Medicine

Link

http://www.nejm.org/doi/pdf/10.1056/NEJM196903202801205

Cited by 47 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hepatocyte-specific deletion of peroxisomal protein PEX13 results in disrupted iron homeostasis;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2020-10

2. Dysregulated hepcidin response to dietary iron in male mice with reduced Gnpat expression;Bioscience Reports;2020-08

3. The evaluation of infants with the Zellweger (cerebro-hepato-renal) syndrome*;Clinical Genetics;2008-04-23

4. Enfermedades peroxisomales: análisis de los niveles de ferritina en el síndrome cerebrohepatorrenal de Zellweger;Revista de Neurología;2008

5. Inborn Errors of Peroxisome Biogenesis and Brain Malformation: Clinical and Biochemical Studies;Congenital Anomalies;1995-03

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