%0 Journal Article
%T 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
%A Kan, T.
%A Takahagi, S.
%A Shindo, H.
%A Tanaka, A.
%A Kawai, M.
%A Hide, M.
%J Clinical and Experimental Dermatology
%V 43
%N 3
%P 329-332
%@ 0307-6938
%D 2018-04-01
%~ DeepDyve