Erythrocyte AMP Deaminase Deficiency in Japanese: A Compound Heterozygote Responsible for the Complete Deficiency
Author:
Publisher
Kluwer Academic Publishers
Link
http://link.springer.com/content/pdf/10.1007/0-306-46843-3_13.pdf
Reference13 articles.
1. Ogasawara, N., Goto, H., Yamada, Y., Watanabe, T. and Asano, T., 1982, AMP deaminase isozymes in human tissues. Biochim. Biophys. Acta 714: 298–306
2. Ogasawara, N., Goto, H., Yamada, Y., and Watanabe, T., 1984, Distribution of AMP deaminase isozymes in various human blood cells. Int. J. Biochem. 16: 269–273.
3. Sabina, R.L., Morisaki, T., Clarke, P., Eddy, R., Shows, T.B., Morton, C.C. and Holmes, E.W., 1990, Characterization of the human and rat myoadenylate deaminase genes. J. Biol. Chem. 265: 9423–9433.
4. Bausch-Junken, M.T., Mahnke-Zizelman, D.K., Morisaki, T. and Sabina, R.L., 1992, Molecular cloning of AMP deaminase isoform L. Sequence and bacterial expression of human AMPD2 cDNA. J. Biol. Chem. 267: 22407–22413.
5. Yamada, Y., Goto, H. and Ogasawara, N., 1992, Cloning and nucleotide sequence of the cDNA encoding human erythrocyte-specific AMP deaminase. Biochim. Biophys. Acta 1171: 125–128.
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