| 1 | AMZ1, BRAT1, CHST12, EIP3B, LFNG, TTYH3, and GNA12
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| Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome?
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| Yu AC, Zambrano RM, Cristian I, Price S, Bernhard B, Zucker M, Venkateswaran S, McGowan-Jordan J, Armour CM.
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| Am J Med Genet A 173(6):1593-1600. doi: 10.1002/ajmg.a.38241. Epub 2017 Apr 25.
2017
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| 2 | AMZ1, AMZ2
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| Identification and characterization of human archaemetzincin-1 and -2, two novel members of a family of metalloproteases widely distributed in Archaea.
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| Diaz-Perales A, Quesada V, Peinado JR, Ugalde AP, Alvarez J, Suarez MF, Gomis-Ruth FX, Lopez-Otin C.
|
| J Biol Chem 280(34):30367-75. Epub 2005 Jun 22. 2005
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