Citations for
1SLC9A7, CHST7, ZNF673
A microdeletion in Xp11.3 accounts for co-segregation of retinitis pigmentosa and mental retardation in a large kindred.
Zhang L, Wang T, Wright AF, Suri M, Schwartz CE, Stevenson RE, Valle D.
Am J Med Genet A 140(4):349-57. 2006
2CHST7
Molecular cloning and expression of a novel chondroitin 6-O-sulfotransferase.
Kitagawa H, Fujita M, Ito N, Sugahara K.
J Biol Chem 275(28):21075-80. 2000