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

T. Kan, S. Takahagi, H. Shindo, A. Tanaka, M. Kawai, M. Hide
  • Clinical and Experimental Dermatology, January 2018, Wiley
  • DOI: 10.1111/ced.13326

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http://dx.doi.org/10.1111/ced.13326

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