Associated Papers
A Novel Mutation p.L461P in KRT5 Causing Localized Epidermolysis Bullosa Simplex.
Jiang X et al.
Annals of Dermatology, 2021
The Position of Targeted Next-generation Sequencing in Epidermolysis Bullosa Diagnosis.
Has C et al.
Acta Dermato-venereologica, 2018
Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotype.
Arin MJ et al.
The British Journal of Dermatology, 2010
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