| 1 | STM |
| Five generations with steatocystoma multiplex congenita: a treatment regimen. | |
| Pamoukian VN, Westreich M. | |
| Plast Reconstr Surg 99(4):1142-6. 1997 | |
| 2 | KRT17, STM |
| Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex. | |
| Smith FJ, Corden LD, Rugg EL, Ratnavel R, Leigh IM, Moss C, Tidman MJ, Hohl D, Huber M, Kunkeler L, Munro CS, Lane EB, McLean WH. | |
| J Invest Dermatol 108(2):220-3. 1997 | |