Cite
MLA Citation
T. Kan et al.. “A unique clinical phenotype of a patient bearing a newly identified deletion mutation in the PSENEN gene along with the pathogenic serum desmoglein‐1 antibody.” Clinical and experimental dermatology, vol. 43, 2018, pp. 329–332. http://access.bl.uk/ark:/81055/vdc_100172209946.0x000014