Related Articles
A novel KRT5 mutation associated with generalized severe epidermolysis bullosa simplex in a 2‑year‑old Chinese boy
Identification of novel <em>KRT5</em> gene variants in two Chinese patients with sporadic form of epidermolysis bullosa simplex: A case report
Novel keratin 5 mutation in a family with epidermolysis bullosa simplex
A novel autosomal partially dominant mutation designated G476D in the keratin 5 gene causing epidermolysis bullosa simplex Weber-Cockayne type: A family study with a genetic twist
A novel frameshift mutation in the <em>FERMT1</em> gene in a Chinese patient with Kindler syndrome