| 1 | MRX19, CLS, RPS6KA3 |
| Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation. | |
| Field M, Tarpey P, Boyle J, Edkins S, Goodship J, Luo Y, Moon J, Teague J, Stratton MR, Futreal PA, Wooster R, Raymond FL, Turner G. | |
| Clin Genet 70(6):509-15. 2006 | |
| 2 | MRX19, RPS6KA3 |
| A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation. | |
| Merienne K, et al. | |
| Nat Genet 22(1):13-4. No abstract available 1999 | |
| 3 | MRX19 |
| Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22. | |
| Donnelly AJ, et al. | |
| Am J Med Genet 51 : 581-585. 1994 | |
| 4 | MRX17, MRX18, MRX19, MRX2 |
| Pericentromeric genes for non-specific X-linked mental retardation (MRX). | |
| Gedeon A, et al. | |
| Am J Med Genet 51 : 553-564. 1994 | |