The Molecular Pathology of Progressive Symmetric Erythrokeratoderma: A Frameshift Mutation in the Loricrin Gene and Perturbations in the Cornified Cell Envelope-Reference-Cited by-同舟云学术

The Molecular Pathology of Progressive Symmetric Erythrokeratoderma: A Frameshift Mutation in the Loricrin Gene and Perturbations in the Cornified Cell Envelope

Published:1997-09 Issue:3 Volume:61 Page:581-589
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ishida-Yamamoto Akemi,McGrath John A.,Lam HaMut,Iizuka Hajime,Friedman Richard A.,Christiano Angela M.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference42 articles.

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2. Autosomal dominant keratoderma, ichthyosiform dermatosis and elevated serum beta-glucuronidase;Camisa;Dermatologica,1988

3. Variant of keratoderma hereditaria mutilans (Vohwinkel's syndrome);Camisa;Arch Dermatol,1984

4. Biochemical, structural, and transglutaminase substrate properties of human loricrin, the major epidermal cornified cell envelope protein;Candi;J Biol Chem,1995

5. Empirical predictions of protein conformation;Chou;Annu Rev Biochem,1978

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