| ［1］ |
Echeverría⁃García B, Vicente A, Hernández Á, et al. Epidermolysis bullosa simplex with mottled pigmentation: a family report and review［J］. Pediatr Dermatol, 2013,30（6）:e125⁃e131. doi: 10.1111/j.1525⁃1470.2012.01748.x.
|
| ［2］ |
Okamura K, Fukushima S, Yamashita J, et al. Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in KRT5［J］. J Dermatol, 2019,46（7）:e233⁃e235. doi: 10.1111/1346⁃8138.14788.
|
| ［3］ |
Irvine AD, Rugg EL, Lane EB, et al. Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation［J］. Br J Dermatol, 2001,144（1）:40⁃45. doi: 10.1046/j.1365⁃2133.2001.03950.x.
|
| ［4］ |
Geller L, Kristal L, Morel KD. Epidermolysis bullosa simplex with mottled pigmentation due to a rare keratin 5 mutation: cutaneous findings in infancy［J］. Pediatr Dermatol, 2013,30（5）:631⁃632. doi: 10.1111/pde.12206.
|
| ［5］ |
Arin MJ, Grimberg G, Schumann H, et al. Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotype［J］. Br J Dermatol, 2010,162（6）:1365⁃1369. doi: 10.1111/j.1365⁃2133.2010.09657.x.
|
| ［6］ |
乌云, 林志淼. 伴斑点状色素沉着的单纯型大疱性表皮松解症一家系基因突变分析［J］. 中国皮肤性病学杂志, 2016,30（2）:111⁃113,135. doi: 10.13735/j.cjdv.1001⁃7089.201508057.
|
