| 1 | DSG1, PPKS1 |
| Mutations in the desmoglein 1 gene in five Pakistani families with striate palmoplantar keratoderma. | |
| Dua-Awereh MB, Shimomura Y, Kraemer L, Wajid M, Christiano AM. | |
| J Dermatol Sci 53(3):192-7. Epub 2009 Jan 20.PMID: 19157795 2009 | |
| 2 | DSG1, PPKS1 |
| Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma. | |
| Hunt DM, Rickman L, Whittock NV, Eady RA, Simrak D, Dopping-Hepenstal PJ, Stevens HP, Armstrong DK, Hennies HC, Kuster W, Hughes AE, Arnemann J, Leigh IM, McGrath JA, Kelsell DP, Buxton RS. | |
| Eur J Hum Genet 9(3):197-203. 2001 | |
| 3 | DSG1, PPKS1 |
| N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma. | |
| Rickman L, et al. | |
| Hum Mol Genet 8(6):971-6. 1999 | |
| 4 | PPKS1 |
| Localization of a locus for the striated form of palmoplantar keratoderma to chromosome 18q near the desmosomal cadherin gene cluster. | |
| Hennies HC, et al. | |
| Hum Mol Genet 4 : 1015-1020. 1995 | |