Epidermolysis bullosa simplex with mottled pigmentation: a novel KRT14 mutation
Document Type
Case ReportPublication Date
2011-08-06Keywords
ChildEpidermolysis 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
Metadata
Show full item recordSource
J Drugs Dermatol. 2011 Aug;10(8):926-7.