Citations for
1DDD, KRT5
A novel heterozygous nonsense mutation of keratin 5 in a Chinese family with Dowling-Degos disease.
Guo L, Luo X, Zhao A, Huang H, Wei Z, Chen L, Qin S, Shao L, Xuan J, Feng G, Minghua C, Luan J, He L, Xing Q.
J Eur Acad Dermatol Venereol 26(7):908-10. doi: 10.1111/j.1468-3083.2011.04115.x. Epub 2011 May 14. 2012
2DDD, KRT5
Loss-of-Function Mutations in the Keratin 5 Gene Lead to Dowling-Degos Disease.
Betz RC, Planko L, Eigelshoven S, Hanneken S, Pasternack SM, Bussow H, Bogaert KV, Wenzel J, Braun-Falco M, Rutten A, Rogers MA, Ruzicka T, Nothen MM, Magin TM, Kruse R.
Am J Hum Genet 78(3):510-9. Epub 2006 Jan 19. 2006