Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolism-Reference-Cited by-同舟云学术

Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolism

Published:2006-02 Issue:2 Volume:27 Page:201-208
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Ferrari Francesca,Foglieni Barbara,Arosio Paolo,Camaschella Clara,Daraio Filomena,Levi Sonia,Antonio García Erce José,Beaumont Carole,Cazzola Mario,Ferrari Maurizio,Cremonesi Laura

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference29 articles.

1. Clinical Severity and Thermodynamic Effects of Iron-responsive Element Mutations in Hereditary Hyperferritinemia-Cataract Syndrome

2. Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataract

3. Identification of New Mutations of the HFE, Hepcidin, and Transferrin Receptor 2 Genes by Denaturing HPLC Analysis of Individuals with Biochemical Indications of Iron Overload

4. Identification of new mutations of hepcidin and hemojuvelin in patients with HFE C282Y allele

5. C29G in the iron-responsive element of l-ferritin: a new mutation associated with hyperferritinemia-cataract

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3. Genetic Disorders Associated with Metal Metabolism;Cells;2019-12-09

4. Hereditary hyperferritinaemia-cataract syndrome (HHCS) – an underestimated condition: ferritin light chain variant spectrum in German families;Clinical Chemistry and Laboratory Medicine (CCLM);2019-06-18

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