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    Goetze, S., Raessler, F., Hipler, U., Schulz, S., Kohlhase, J., & Elsner, P. (n.d.). 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. Journal of the European Academy of Dermatology and Venereology, 30, 493–494. http://access.bl.uk/ark:/81055/vdc_100030761721.0x000032