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Year | Number of Results |
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1987 | 1 |
1992 | 1 |
1994 | 1 |
1997 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 416697
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Genomic organization of Ampd3, heart-type AMPD gene, located in mouse chromosome 7.
Mamm Genome. 1997 Oct;8(10):767-9. doi: 10.1007/s003359900562.
Mamm Genome. 1997.
PMID: 9321472
No abstract available.
A point mutation responsible for human erythrocyte AMP deaminase deficiency.
Yamada Y, Goto H, Ogasawara N.
Yamada Y, et al.
Hum Mol Genet. 1994 Feb;3(2):331-4. doi: 10.1093/hmg/3.2.331.
Hum Mol Genet. 1994.
PMID: 8004104
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Deficiency of AMP deaminase in erythrocytes.
Ogasawara N, Goto H, Yamada Y, Nishigaki I, Itoh T, Hasegawa I, Park KS.
Ogasawara N, et al.
Hum Genet. 1987 Jan;75(1):15-8. doi: 10.1007/BF00273831.
Hum Genet. 1987.
PMID: 3804327
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Cloning and nucleotide sequence of the cDNA encoding human erythrocyte-specific AMP deaminase.
Yamada Y, Goto H, Ogasawara N.
Yamada Y, et al.
Biochim Biophys Acta. 1992 Nov 15;1171(1):125-8. doi: 10.1016/0167-4781(92)90153-q.
Biochim Biophys Acta. 1992.
PMID: 1420359
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