| 1 | FPH2, KITLG |
| KITLG mutations cause familial progressive hyper- and hypopigmentation. | |
| Amyere M, Vogt T, Hoo J, Brandrup F, Bygum A, Boon L, Vikkula M. | |
| J Invest Dermatol 131(6):1234-9. doi: 10.1038/jid.2011.29. Epub 2011 Mar 3. 2011 | |
| 2 | FPH2, KITLG |
| Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation. | |
| Wang ZQ, Si L, Tang Q, Lin D, Fu Z, Zhang J, Cui B, Zhu Y, Kong X, Deng M, Xia Y, Xu H, Le W, Hu L, Kong X. | |
| Am J Hum Genet 84(5):672-7. Epub 2009 Apr 16. 2009 | |