Epidermolysis bullosa simplex with mottled pigmentation: a novel KRT14 mutation
Department of Medicine, Division of Dermatology; Department of Pediatrics
Child; Epidermolysis Bullosa Simplex; Humans; Keratin-14; Male; Pigmentation Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Dermatology | Diagnosis | Genetic Phenomena | Pathological Conditions, Signs and Symptoms | Pediatrics | Skin and Connective Tissue Diseases
J Drugs Dermatol. 2011 Aug;10(8):926-7.
Journal of drugs in dermatology : JDD
Gray C, Greenlaw SM, Alavian C, Wiss K. (2011). Epidermolysis bullosa simplex with mottled pigmentation: a novel KRT14 mutation. Dermatology Publications. Retrieved from https://escholarship.umassmed.edu/derm_pubs/64