Inflammatory Peeling Skin Syndrome Caused by a Mutation in CDSN Encoding Corneodesmosin
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference18 articles.
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2. A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin;Caubet;FASEB J,2010
3. Homo-oligomerization of human corneodesmosin is mediated by its N-terminal glycine loop domain;Caubet;J Invest Dermatol,2004
4. Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome;Chavanas;Nat Genet,2000
5. A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming;Fallon;Nat Genet,2009
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