Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT5

JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY

WILEY

1. Practical Research Project for Rare/Intractable Diseases from Japan Agency for Medical Research and Development, AMED [16ek0109067h0003]