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A loss-of-function NCSTN mutation associated with familial Dowling Degos disease and hidradenitis suppurativa

Document Type

Article

Author

de Oliveira, A.S.L.E.; Brandão, L.A.C.; de Siqueira, R.C.; de Fátima Medeiros Brito, M.; Nait-Meddour, C.; Jamain, S.; Boniotto, M.; Tricarico, P.M.; Moura, R.; d'Adamo, A.P.; Agrelli, A.; Crovella, S.

Source

In: Experimental Dermatology. (Experimental Dermatology, November 2023, 32(11):1935-1945)

Subject

Language

English

ISSN

16000625
09066705

Online Access

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Scopus Find it@PNU

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