Unexpected manifestation of naevoid basal cell carcinoma (Gorlin) syndrome with a novel mutation in the PTCH1 gene in a female patient with long‐lasting pemphigus vulgaris. (20th January 2015) - Goetze, S.; Raessler, F.; Hipler, U.C.; Schulz, S.; Kohlhase, J.; Elsner, P.