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 unique clinical phenotype of a patient bearing a newly identified deletion mutation in the PSENEN gene along with the pathogenic serum desmoglein‐1 antibody

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Bibliographic Details
Published in:Clinical and experimental dermatology Vol. 43; no. 3; pp. 329 - 332
Main Authors: Kan, T., Takahagi, S., Shindo, H., Tanaka, A., Kawai, M., Hide, M.
Format: Journal Article
Language:English
Published: England Oxford University Press 01-04-2018
Subjects:
Gene deletion
Online Access:Get full text
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Description
ISSN:0307-6938
1365-2230
DOI:10.1111/ced.13326