Gene Mutations for Human Erythrocyte AMP Deaminase Deficiency-Reference-Cited by-同舟云学术

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Gene Mutations for Human Erythrocyte AMP Deaminase Deficiency

Published:1995 Issue: Volume: Page:703-706
ISSN:0065-2598
Container-title:Purine and Pyrimidine Metabolism in Man VIII
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Author:

Yamada Yasukazu,Goto Haruko,Murase Takaji,Ogasawara Nobuaki

Publisher

Springer US

Link

http://link.springer.com/content/pdf/10.1007/978-1-4615-2584-4_146

Reference14 articles.

1. N. Ogasawara, H. Goto, Y. Yamada, T. Watanabe and T. Asano, AMP deaminase isozymes in human tissues., Biochim. Biophys. Acta 714:298 (1982).

2. N. Ogasawara, H. Goto, Y. Yamada, and T. Watanabe, Distribution of AMP deaminase isozymes in various human blood cells., Int. J. Biochem. 16:269 (1984).

3. R.L. Sabina, R. Marquetant, N.M. Desai, K. Kaletha, and E.W. Holmes, Cloning and sequence of rat myoadenylate deaminase cDNA: evidence for tissue-specific and developmental regulation., J. Biol. Chem. 262:12397 (1987).

4. R.L. Sabina, T. Morisaki, P. Clarke, R. Eddy, T.B. Shows, C.C. Morton, and E.W. Holmes, Characterization of the human and rat myoadenylate deaminase genes., J. Biol. Chem. 265:9423 (1990).

5. T. Morisaki, R.L. Sabina, and E.W. Holmes, Adenylate deaminase: a multigene family in humans and rats., J. Biol. Chem. 265:11482 (1990).

Cited by 1 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. Proteinuria in AMPD2-deficient mice;Genes to Cells;2011-12-29

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