Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosis
Author:
Affiliation:
1. Ankara University Biotechnology Institute; Ankara Turkey
2. Department; of Child Health and Diseases; TOBB University; Ankara Turkey
3. Department of Hematology, Medical School; Namik Kemal University; Tekirdag Turkey
Funder
Scientific and Technological Research Council of Turkey
Publisher
Wiley
Subject
Clinical Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/prca.201200010/fullpdf
Reference51 articles.
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3. Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosis;Coetzer;Blood,1987
4. Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin;Glele-Kakai;Br. J. Haematol.,1996
5. Red-cell cytoskeletal abnormalities-implications for malaria;Nagel;N. Engl. J. Med.,1990
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