In partnership with:
This shareable PDF can be hosted on any platform or network and is fully compliant with publisher copyright.
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