Citations for
1CDM1, CDM2, KRT12, KRT13, KRT14, KRT3, KRT5, KTRT4, WHSN1, WHSN2
The molecular basis of human keratin disorders.
Arin MJ.
Hum Genet 125(4):355-73. Epub 2009 Feb 27. Review. 2009
2CDM1, CDM2, KRT3, KRT12
Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy.
Irvine AD, Corden LD, Swensson O, Swensson B, Moore JE, Frazer DG, Smith FJ, Knowlton RG, Christophers E, Rochels R, Uitto J, McLean WH.
Nat Genet 16(2):184-7. 1997