Human Factors Engineering Mutation and Hepcidin in Beta-Thalasseima : Thalassemia,Hfe gene,Hereditary hemochromatosis,iron metabolism,hepcidin

Language: English

Published by Scholars' Press

6202308931 / 9786202308939

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Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH

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Softcover

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Item description from seller

nach der Bestellung gedruckt Neuware - Printed after ordering - Thalassemia is an important hematological disorder. The possibility of iron overload development may be increase by Interaction between thalassemia and HFE gene mutations. This study aim to investigate the possible association between serum hepcidin level as indicator of iron concentration and the presence of HFE gene mutations. Excess iron overload increases the risk of liver cirrhosis,cancer,hypogonadism,arthritis, cardiac arrhythmia, heart failure, retinal degeneration, diabetes mellitus, neurodegenerative diseases (Alzheimer's,Parkinson's, Huntington's), and premature death.

Seller Inventory # 9786202308939

Bibliographic details

Title
Human Factors Engineering Mutation and Hepcidin in Beta-Thalasseima : Thalassemia,Hfe gene,Hereditary hemochromatosis,iron metabolism,hepcidin
Author
Sara Rabea Ibrahim Saad El-dien
Publisher
Scholars' Press
Condition
Neu
Binding
Taschenbuch
Language
English
ISBN 10
6202308931
ISBN 13
9786202308939
Item weight
227 grams
Dimensions
220x150x9 mm

AHA-BUCH GmbH

Einbeck, Germany

5-star seller

AbeBooks seller since August 14, 2006

Shipping rates from Germany to U.S.A.

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