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A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 7, p. 1133, doi. 10.1093/hmg/ddl028
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- Article
A Novel Substitution in Keratin 10 in Epidermolytic Hyperkeratosis.
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- Journal of Investigative Dermatology, 1999, v. 112, n. 4, p. 506, doi. 10.1046/j.1523-1747.1999.00557.x
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- Article
A Novel Mutation in the 1A Domain of Keratin 2e in Ichthyosis Bullosa of Siemens.
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- Journal of Investigative Dermatology, 1999, v. 112, n. 3, p. 380, doi. 10.1046/j.1523-1747.1999.00529.x
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- Article
Inducible Mouse Models for Inherited Skin Diseases: Implications for Skin Gene Therapy.
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- Cells Tissues Organs, 2004, v. 177, n. 3, p. 160, doi. 10.1159/000079990
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- Article
Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.
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- Human Mutation, 2006, v. 27, n. 7, p. 719, doi. 10.1002/humu.9437
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- Article
Recessive Epidermolytic Hyperkeratosis Caused by a Previously Unreported Termination Codon Mutation in the Keratin 10 Gene.
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- Journal of Investigative Dermatology, 2009, v. 129, n. 11, p. 2721, doi. 10.1038/jid.2009.131
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- Article
Focal Activation of a Mutant Allele Defines the Role of Stem Cells in Mosaic Skin Disorders.
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- Journal of Cell Biology, 2001, v. 152, n. 3, p. 645, doi. 10.1083/jcb.152.3.645
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- Article