6 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 21811984 | [Mutation analysis of KRT10 gene in a patient with bullous congenital ichthyosiform erythroderma]. | 2011 Aug | 1 |
2 | 11204523 | Recurrent R156H mutation of KRT10 in a Japanese family with bullous congenital ichthyosiform erythroderma. | 2000 Jul | 1 |
3 | 9742571 | Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis. | 1998 Aug | 1 |
4 | 9184002 | A keratin K10 gene mutation in a Japanese patient with epidermolytic hyperkeratosis. | 1997 Mar | 3 |
5 | 7508181 | Preferential sites in keratin 10 that are mutated in epidermolytic hyperkeratosis. | 1994 Feb | 1 |
6 | 7512983 | Genetic mutations in the K1 and K10 genes of patients with epidermolytic hyperkeratosis. Correlation between location and disease severity. | 1994 Apr | 1 |