| 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 | CHST11, CHST12
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| Molecular cloning and expression of chondroitin 4-sulfotransferase.
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| Yamauchi S, Mita S, Matsubara T, Fukuta M, Habuchi H, Kimata K, Habuchi O.
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| J Biol Chem 275(12):8975-81. 2000
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| 3 | B3GAT1, CHST11, CHST1, CHST12, CHST10
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| Molecular cloning and expression of two distinct human chondroitin 4-O-sulfotransferases that belong to the HNK-1 sulfotransferase gene family.
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| Hiraoka N, Nakagawa H, Ong E, Akama TO, Fukuda MN, Fukuda M.
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| J Biol Chem 275(26):20188-96. 2000
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