Loss of Corneodesmosin Leads to Severe Skin Barrier Defect, Pruritus, and Atopy: Unraveling the Peeling Skin Disease-Reference-Cited by-同舟云学术

Loss of Corneodesmosin Leads to Severe Skin Barrier Defect, Pruritus, and Atopy: Unraveling the Peeling Skin Disease

Published:2010-08 Issue:2 Volume:87 Page:274-281
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Oji Vinzenz,Eckl Katja-Martina,Aufenvenne Karin,Nätebus Marc,Tarinski Tatjana,Ackermann Katharina,Seller Natalia,Metze Dieter,Nürnberg Gudrun,Fölster-Holst Regina,Schäfer-Korting Monika,Hausser Ingrid,Traupe Heiko,Hennies Hans Christian

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference39 articles.

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3. A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming;Fallon;Nat. Genet.,2009

4. The peeling skin syndrome;Levy;J. Am. Acad. Dermatol.,1982

5. The Ichthyoses. A Guide to Clinical Diagnosis, Genetic Counseling, and Therapy;Traupe,1989

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