Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family

Lignende værker

• Neonatal Epidermolytic Ichthyosis Caused by a KRT10 Mutation (c.467G>A, p.Arg156His): A Case Report
  af: Elke Smits, et al.
  Udgivet: (2025-08-01)
• Mutations in KRT10 in epidermolytic acanthoma
  af: Cheraghlou, Shayan, et al.
  Udgivet: (2020)
• Annular epidermolytic ichthyosis: An exceptional mild subtype of epidermolytic ichthyosis without genotype and phenotype correlation
  af: Reolid, Alejandra, et al.
  Udgivet: (2019)
• A p.478I>T KRT1 mutation in a case of annular epidermolytic ichthyosis
  af: Zaki, Theodore D., et al.
  Udgivet: (2018)
• Mosaic epidermolytic ichthyosis
  af: Mendes, Sónia Raquel, et al.
  Udgivet: (2021)