Citations for
1DSG1, 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
2DSG1, 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
3DSG1, 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
4PPKS1
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